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	<title>Polypyridine complex - Revision history</title>
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	<updated>2026-05-11T15:56:38Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<title>imported&gt;Zumedi: typo</title>
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		<updated>2025-02-04T14:40:50Z</updated>

		<summary type="html">&lt;p&gt;typo&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Polypyridine complexes&amp;#039;&amp;#039;&amp;#039; are [[coordination complex]]es containing polypyridine ligands, such as [[2,2&amp;#039;-bipyridine]], 1,10-[[phenanthroline]], or 2,2&amp;#039;;6&amp;#039;2&amp;quot;-[[terpyridine]].&lt;br /&gt;
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Polypyridines are multidentate [[ligand]]s that confer characteristic properties to the metal complexes that they form.  Some complexes strongly absorb light via a process called metal-to-ligand [[Intervalence charge transfer|charge transfer]] (MLCT).&amp;lt;ref&amp;gt;Balzani, V., Juris, A., &amp;quot;Photochemistry and photophysics of Ru(II)-polypyridine complexes in the Bologna group. From early studies to recent developments&amp;quot;, Coord. Chem. Rev. 2001, 211, 97.  {{doi|10.1016/S0010-8545(00)00274-5}}.&amp;lt;/ref&amp;gt;  The properties of these complexes can be tuned by changes in substituents.  For example, electron donation, electron withdrawal, and π-conjugating groups, to the polypyridine [[Moiety (chemistry)|moiety]]. The MLCT absorption band can be shifted, the emission wavelength can be changed, and the emission lifetime can be extended.&amp;lt;ref&amp;gt;Hammarstroem, L., Johansson, O., &amp;quot;Expanded bite angles in tridentate ligands. Improving the photophysical properties in bistridentate Ru&amp;lt;sup&amp;gt;II&amp;lt;/sup&amp;gt; polypyridine complexes&amp;quot;, Coord. Chem. Rev. 2010, 254, 2546.  {{doi|10.1016/j.ccr.2010.01.006}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
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[[File:Tris(bipyridine)ruthenium(II) chloride.png|thumb|right|224px|[[Tris(bipyridine)ruthenium(II) chloride|Tris(bipyridine)ruthenium(II)]] is the preeminent example of a polypyridine complex.]]&lt;br /&gt;
&lt;br /&gt;
A well-known example of a polypyridine complex is the tris(bipyridine) derivative of ruthenium(II), [Ru(bpy)&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;]&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;. This complex exhibits intense [[luminescence]] at room temperature in aqueous solution. Another example is a platinum-bipyridine-dithiolate complex, Pt(bpy)(bdt), in which bdt denotes a 1,2-benzenedithiolate [[ion|anion]]. This complex also exhibits [[Fluorescence|photoluminescence]] at room temperature, and its wavelength and lifetime can be tuned by substitution of either bipyridine or dithiolate moieties. Structural control is easier than for [[ruthenium]] complexes due to the square planar structure of the [[platinum]] complex.&lt;br /&gt;
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Some other areas of investigation involves immobilizing these complexes on electrodes.&amp;lt;ref&amp;gt;Zhong, Y.-W., Yao, C.-J., Nie, H.-J., &amp;quot;Electropolymerized films of vinyl-substituted polypyridine complexes: Synthesis, characterization, and applications&amp;quot;, Coord. Chem. Rev. 2013, 257, 1357.  {{doi|10.1016/j.ccr.2013.01.001}}&amp;lt;/ref&amp;gt;  Some polypyridyl complexes intercalate into [[DNA]] and show promise as drugs.&amp;lt;ref&amp;gt;Komor, Alexis C.; Barton, Jacqueline K. &amp;quot;The path for metal complexes to a DNA target&amp;quot; Chemical Communications 2013, vol. 49, 3617-3630. {{doi|10.1039/c3cc00177f}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
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==See also==&lt;br /&gt;
* [[Transition metal complexes of 2,2&amp;#039;-bipyridine]]&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;br /&gt;
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{{DEFAULTSORT:Polypyridine Complex}}&lt;br /&gt;
[[Category:Bipyridines]]&lt;/div&gt;</summary>
		<author><name>imported&gt;Zumedi</name></author>
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