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	<title>Bipyridine - Revision history</title>
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	<updated>2026-04-22T00:02:40Z</updated>
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	<entry>
		<id>https://wikimd.com/index.php?title=Bipyridine&amp;diff=6416499&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2025-03-03T05:29:20Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&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 05:29, 3 March 2025&lt;/td&gt;
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		<author><name>Prab</name></author>
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		<title>Prab: CSV import</title>
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		<updated>2024-03-25T02:54:29Z</updated>

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&amp;#039;&amp;#039;&amp;#039;Bipyridine‏‎&amp;#039;&amp;#039;&amp;#039; is an [[organic compound]] with the chemical formula (C₅H₄N)₂. It is a colorless solid that is soluble in organic solvents. Bipyridine is a bidentate [[ligand]] that is widely used in [[coordination chemistry]]. It has two pyridine rings connected by a single bond. The molecule is planar and belongs to the point group D₂h. Bipyridine and its derivatives are used as ligands in many [[transition metal]] complexes.&lt;br /&gt;
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The most common derivatives of bipyridine include 2,2&amp;#039;-bipyridine (often abbreviated as bipy or bpy), which is the simplest member of the bipyridine family, and 4,4&amp;#039;-bipyridine. These compounds are important in the field of [[inorganic chemistry]] for the synthesis of coordination complexes, due to their ability to donate two electrons to a metal center through the nitrogen atoms present in the pyridine rings.&lt;br /&gt;
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Bipyridine complexes have been extensively studied for their [[electronic properties]], [[catalysis|catalytic activities]], and potential applications in [[materials science]], [[photovoltaics]], and as components in [[molecular electronics]]. For example, complexes containing bipyridine ligands are used in the Grätzel cell, a type of [[solar cell]], for the conversion of solar energy into electrical energy.&lt;br /&gt;
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In addition to its applications in coordination chemistry, bipyridine is also used as a building block in [[supramolecular chemistry]] for the construction of more complex molecular architectures through hydrogen bonding, π-π stacking, and metal coordination interactions.&lt;br /&gt;
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== Synthesis ==&lt;br /&gt;
Bipyridine is synthesized through the dehydrogenation of pyridine, usually using a metal catalyst such as [[nickel]] or [[palladium]]. The reaction involves the formation of a carbon-carbon bond between two pyridine molecules.&lt;br /&gt;
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== Applications ==&lt;br /&gt;
### Coordination Chemistry ###&lt;br /&gt;
Bipyridine ligands form stable complexes with most transition metals. These complexes are involved in various catalytic processes, including the [[oxidation]] and [[reduction]] reactions that are fundamental to [[electrochemistry]] and [[photochemistry]].&lt;br /&gt;
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### Materials Science ###&lt;br /&gt;
In materials science, bipyridine complexes are studied for their optical and electronic properties, making them potential candidates for use in organic light-emitting diodes (OLEDs), solar cells, and molecular electronics.&lt;br /&gt;
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### Supramolecular Chemistry ###&lt;br /&gt;
Bipyridine derivatives are used as building blocks in supramolecular chemistry to create complex structures with specific functions, such as molecular recognition, self-assembly, and the construction of molecular machines.&lt;br /&gt;
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== Safety ==&lt;br /&gt;
Bipyridine is considered to be moderately toxic. It should be handled with care, using appropriate safety precautions to avoid ingestion, inhalation, or skin contact.&lt;br /&gt;
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[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Ligands]]&lt;br /&gt;
[[Category:Coordination chemistry]]&lt;br /&gt;
[[Category:Supramolecular chemistry]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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