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	<title>Vezna izomerija - Revision history</title>
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	<updated>2026-05-24T05:53:26Z</updated>
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		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21444&amp;oldid=prev</id>
		<title>FilipK at 11:31, 6 January 2023</title>
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		<updated>2023-01-06T11:31:41Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 11:31, 6 January 2023&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l9&quot;&gt;Line 9:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 9:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;*sulfit, SO&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;2-&amp;lt;/sup&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;*sulfit, SO&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;2-&amp;lt;/sup&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Primeri veznih izomerov so vijolično obarvani [(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;Co-SCN]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; in oranžno obarvani [(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;Co-NCS]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Izomerizacija S-veznega izomera v N-vezni izomer poteka intramolekularno.&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[1]&lt;/del&gt;&amp;lt;ref&amp;gt;Buckingham, D. A.; Creaser, I. I.; Sargeson, A. M. (1970). &quot;Mechanism of Base Hydrolysis for Co&amp;lt;sup&amp;gt;III&amp;lt;/sup&amp;gt;(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;X&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; Ions. Hydrolysis and Rearrangement for the Sulfur-Bonded Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;SCN&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; Ion&quot;. &#039;&#039;Inorg. Chem.&#039;&#039; &#039;&#039;&#039;9&#039;&#039;&#039; (3): 655–661. doi:[https://doi.org/10.1021%2Fic50085a044 10.1021/ic50085a044]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Primeri veznih izomerov so vijolično obarvani [(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;Co-SCN]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; in oranžno obarvani [(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;Co-NCS]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Izomerizacija S-veznega izomera v N-vezni izomer poteka intramolekularno.&amp;lt;ref&amp;gt;Buckingham, D. A.; Creaser, I. I.; Sargeson, A. M. (1970). &quot;Mechanism of Base Hydrolysis for Co&amp;lt;sup&amp;gt;III&amp;lt;/sup&amp;gt;(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;X&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; Ions. Hydrolysis and Rearrangement for the Sulfur-Bonded Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;SCN&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; Ion&quot;. &#039;&#039;Inorg. Chem.&#039;&#039; &#039;&#039;&#039;9&#039;&#039;&#039; (3): 655–661. doi:[https://doi.org/10.1021%2Fic50085a044 10.1021/ic50085a044]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Kompleks &amp;#039;&amp;#039;cis&amp;#039;&amp;#039;-diklorotetrakis(dimetilsulfoksid)rutenij(II) [RuCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;(dmso)&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;] ima vezne izomere dimetilsulfoksidnih ligandov (vezava preko žvepla ali preko kisika). &amp;#039;&amp;#039;Trans&amp;#039;&amp;#039;-diklorotetrakis(dimetilsulfoksid)rutenij(II) ne kaže veznih izomerov.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Kompleks &amp;#039;&amp;#039;cis&amp;#039;&amp;#039;-diklorotetrakis(dimetilsulfoksid)rutenij(II) [RuCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;(dmso)&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;] ima vezne izomere dimetilsulfoksidnih ligandov (vezava preko žvepla ali preko kisika). &amp;#039;&amp;#039;Trans&amp;#039;&amp;#039;-diklorotetrakis(dimetilsulfoksid)rutenij(II) ne kaže veznih izomerov.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[2]&lt;/del&gt;&amp;lt;ref&amp;gt;Werner, A. (1907). &quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&quot;. &#039;&#039;Ber.&#039;&#039; &#039;&#039;&#039;40&#039;&#039;&#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[3]&lt;/del&gt;&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&quot;. &#039;&#039;Inorganic Chemistry.&#039;&#039; &#039;&#039;&#039;1&#039;&#039;&#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.&amp;lt;ref&amp;gt;Werner, A. (1907). &quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&quot;. &#039;&#039;Ber.&#039;&#039; &#039;&#039;&#039;40&#039;&#039;&#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&quot;. &#039;&#039;Inorganic Chemistry.&#039;&#039; &#039;&#039;&#039;1&#039;&#039;&#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.[https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png (slika)]]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.[https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png (slika)]]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>FilipK</name></author>
	</entry>
	<entry>
		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21443&amp;oldid=prev</id>
		<title>FilipK at 11:28, 6 January 2023</title>
		<link rel="alternate" type="text/html" href="https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21443&amp;oldid=prev"/>
		<updated>2023-01-06T11:28:33Z</updated>

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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 11:28, 6 January 2023&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l15&quot;&gt;Line 15:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 15:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.[2]&amp;lt;ref&amp;gt;Werner, A. (1907). &amp;quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&amp;quot;. &amp;#039;&amp;#039;Ber.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;40&amp;#039;&amp;#039;&amp;#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.[3]&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &amp;quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.[2]&amp;lt;ref&amp;gt;Werner, A. (1907). &amp;quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&amp;quot;. &amp;#039;&amp;#039;Ber.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;40&amp;#039;&amp;#039;&amp;#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.[3]&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &amp;quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png (slika)]&lt;/ins&gt;]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>FilipK</name></author>
	</entry>
	<entry>
		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21442&amp;oldid=prev</id>
		<title>FilipK: Undo revision 21441 by FilipK (Talk)</title>
		<link rel="alternate" type="text/html" href="https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21442&amp;oldid=prev"/>
		<updated>2023-01-06T11:25:42Z</updated>

		<summary type="html">&lt;p&gt;Undo revision 21441 by &lt;a href=&quot;/index.php?title=Special:Contributions/FilipK&quot; title=&quot;Special:Contributions/FilipK&quot;&gt;FilipK&lt;/a&gt; (&lt;a href=&quot;/index.php?title=User_talk:FilipK&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;User talk:FilipK (page does not exist)&quot;&gt;Talk&lt;/a&gt;)&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 11:25, 6 January 2023&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l15&quot;&gt;Line 15:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 15:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.[2]&amp;lt;ref&amp;gt;Werner, A. (1907). &amp;quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&amp;quot;. &amp;#039;&amp;#039;Ber.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;40&amp;#039;&amp;#039;&amp;#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.[3]&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &amp;quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.[2]&amp;lt;ref&amp;gt;Werner, A. (1907). &amp;quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&amp;quot;. &amp;#039;&amp;#039;Ber.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;40&amp;#039;&amp;#039;&amp;#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.[3]&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &amp;quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;VeznaIzomera&lt;/del&gt;.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers&lt;/ins&gt;.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>FilipK</name></author>
	</entry>
	<entry>
		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21441&amp;oldid=prev</id>
		<title>FilipK at 11:24, 6 January 2023</title>
		<link rel="alternate" type="text/html" href="https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21441&amp;oldid=prev"/>
		<updated>2023-01-06T11:24:50Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 11:24, 6 January 2023&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l15&quot;&gt;Line 15:&lt;/td&gt;
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&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Zgodovina ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.[2]&amp;lt;ref&amp;gt;Werner, A. (1907). &amp;quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&amp;quot;. &amp;#039;&amp;#039;Ber.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;40&amp;#039;&amp;#039;&amp;#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.[3]&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &amp;quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.[2]&amp;lt;ref&amp;gt;Werner, A. (1907). &amp;quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&amp;quot;. &amp;#039;&amp;#039;Ber.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;40&amp;#039;&amp;#039;&amp;#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.[3]&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &amp;quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers&lt;/del&gt;.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Image:&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;VeznaIzomera&lt;/ins&gt;.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Viri ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;lt;references /&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>FilipK</name></author>
	</entry>
	<entry>
		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Vezna_izomerija&amp;diff=21439&amp;oldid=prev</id>
		<title>FilipK: New page: &#039;&#039;Povzeto po &#039;&#039;&#039;Linkage isomerism&#039;&#039;&#039; from Wikipedia, the free encyclopedia:&#039;&#039; https://en.wikipedia.org/wiki/Linkage_isomerism  V kemiji je &#039;&#039;&#039;vezna izomerija&#039;&#039;&#039; oblika izomerije, kjer imaj...</title>
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		<updated>2023-01-06T10:56:30Z</updated>

		<summary type="html">&lt;p&gt;New page: &amp;#039;&amp;#039;Povzeto po &amp;#039;&amp;#039;&amp;#039;Linkage isomerism&amp;#039;&amp;#039;&amp;#039; from Wikipedia, the free encyclopedia:&amp;#039;&amp;#039; https://en.wikipedia.org/wiki/Linkage_isomerism  V kemiji je &amp;#039;&amp;#039;&amp;#039;vezna izomerija&amp;#039;&amp;#039;&amp;#039; oblika izomerije, kjer imaj...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;Povzeto po &amp;#039;&amp;#039;&amp;#039;Linkage isomerism&amp;#039;&amp;#039;&amp;#039; from Wikipedia, the free encyclopedia:&amp;#039;&amp;#039; https://en.wikipedia.org/wiki/Linkage_isomerism&lt;br /&gt;
&lt;br /&gt;
V kemiji je &amp;#039;&amp;#039;&amp;#039;vezna izomerija&amp;#039;&amp;#039;&amp;#039; oblika izomerije, kjer imajo določene koordinacijske spojine enako sestavo, vendar se razlikujejo po načinu vezave kovinskega atoma z ligandom.&lt;br /&gt;
&lt;br /&gt;
Tipični ligandi, odgovorni za nastanek veznih izomerov, so:&lt;br /&gt;
*tiocianat, SCN&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; – izotiocianat, NCS&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt;&lt;br /&gt;
*selenocianat, SeCN&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; – izoselenocianat, NCSe&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt;&lt;br /&gt;
*nitrit, NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt;&lt;br /&gt;
*sulfit, SO&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;2-&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Primeri veznih izomerov so vijolično obarvani [(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;Co-SCN]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; in oranžno obarvani [(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;Co-NCS]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Izomerizacija S-veznega izomera v N-vezni izomer poteka intramolekularno.[1]&amp;lt;ref&amp;gt;Buckingham, D. A.; Creaser, I. I.; Sargeson, A. M. (1970). &amp;quot;Mechanism of Base Hydrolysis for Co&amp;lt;sup&amp;gt;III&amp;lt;/sup&amp;gt;(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;X&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; Ions. Hydrolysis and Rearrangement for the Sulfur-Bonded Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;SCN&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt; Ion&amp;quot;. &amp;#039;&amp;#039;Inorg. Chem.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;9&amp;#039;&amp;#039;&amp;#039; (3): 655–661. doi:[https://doi.org/10.1021%2Fic50085a044 10.1021/ic50085a044]&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Kompleks &amp;#039;&amp;#039;cis&amp;#039;&amp;#039;-diklorotetrakis(dimetilsulfoksid)rutenij(II) [RuCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;(dmso)&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;] ima vezne izomere dimetilsulfoksidnih ligandov (vezava preko žvepla ali preko kisika). &amp;#039;&amp;#039;Trans&amp;#039;&amp;#039;-diklorotetrakis(dimetilsulfoksid)rutenij(II) ne kaže veznih izomerov.&lt;br /&gt;
&lt;br /&gt;
== Zgodovina ==&lt;br /&gt;
Vezna izomerija je bila prvič opažena pri pentaaminnitrokobaltovem(III) kloridu, [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Ta kationski kobaltov kompleks je mogoče izolirati v obliki obeh veznih izomerov. V rumeno obarvanem izomeru je nitro ligand vezan preko dušika. V rdečem veznem izomeru je nitrito vezan preko enega atoma kisika. O-vezni izomer je pogosto zapisan kot [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(ONO)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. Čeprav je bil obstoj izomerov znan že proti koncu 19. stoletja, je bila razlika pojasnjena šele leta 1907.[2]&amp;lt;ref&amp;gt;Werner, A. (1907). &amp;quot;Über strukturisomere Salze der Rhodanwasserstoffsäure und der salpetrigen Säure&amp;quot;. &amp;#039;&amp;#039;Ber.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;40&amp;#039;&amp;#039;&amp;#039; (1): 765–788. doi:[https://doi.org/10.1002%2Fcber.190704001117 10.1002/cber.190704001117]&amp;lt;/ref&amp;gt; Kasneje je bilo dokazano, da se rdeči izomer pretvori v rumeni izomer po UV-sevanju. V tem posebnem primeru pride do tvorbe nitro izomera (Co-NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;) iz nitrito izomera (Co-ONO) z intramolekularno preureditvijo.[3]&amp;lt;ref&amp;gt;Basolo, Fred; Hammaker, G.S (1 February 1962). &amp;quot;Synthesis and Isomerization of Nitritopentammine Complexes of Rhodium(III), Iridium(III), and Platinum(IV)&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry.&amp;#039;&amp;#039; &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039; (1): 1–5. doi:[https://doi.org/10.1021%2Fic50001a001 10.1021/ic50001a001]&amp;lt;/ref&amp;gt;&lt;br /&gt;
[[Image:https://en.wikipedia.org/wiki/Linkage_isomerism#/media/File:LinkageIsomers.png|thumb|300px|center|Strukture dveh veznih izomerov [Co(NH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;(NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;)]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
== Viri ==&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;/div&gt;</summary>
		<author><name>FilipK</name></author>
	</entry>
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