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  2. Bipyridine - Wikipedia

    en.wikipedia.org/wiki/Bipyridine

    Bipyridines are a family of organic compounds with the formula (C 5 H 4 N) 2, consisting of two pyridyl (C 5 H 4 N) rings. Pyridine is an aromatic nitrogen-containing heterocycle. The bipyridines are all colourless solids, which are soluble in organic solvents and slightly soluble in water. Bipyridines, especially the 4,4' isomer, are mainly of ...

  3. Category:Bipyridines - Wikipedia

    en.wikipedia.org/wiki/Category:Bipyridines

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  4. 2,2′-Bipyridine - Wikipedia

    en.wikipedia.org/wiki/2,2′-Bipyridine

    Bahasa Indonesia; Italiano; Magyar ... Unsymmetrically substituted 2,2'-bipyridines can be prepared by cross coupling reaction of 2 ... Wikipedia® is a registered ...

  5. Desk - Wikipedia

    en.wikipedia.org/wiki/Desk

    Desk; c. 1765; mahogany, chestnut and tulip poplar; 87.3 x 92.7 x 52.1 cm; Metropolitan Museum of Art (New York City) A desk or bureau is a piece of furniture with a flat table-style work surface used in a school, office, home or the like for academic, professional or domestic activities such as reading, writing, or using equipment such as a computer.

  6. 4,4'-Bipyridine - Wikipedia

    en.wikipedia.org/wiki/4,4'-Bipyridine

    4,4′-Bipyridine was first obtained in 1868 by the Scottish chemist Thomas Anderson via heating pyridine with sodium metal. [1] However, Anderson's empirical formula for 4,4′-bipyridine was incorrect. [2]

  7. BTBP - Wikipedia

    en.wikipedia.org/wiki/BTBP

    The bis-triazinyl bipyridines (BTBPs) are a class of chemical compounds which are tetradentate ligands similar in shape to quaterpyridine. The BTBPs are made by the reaction of hydrazine and a 1,2-diketone (such as hexane-3,4-dione ) with 6,6'-di cyano -2,2'-bipyridine.

  8. Category:Pyridines - Wikipedia

    en.wikipedia.org/wiki/Category:Pyridines

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  9. Transition metal complexes of 2,2'-bipyridine - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Many ring-substituted variants of bipy have been described, especially dimethyl-2,2'-bipyridines. [6] [7] Alkyl substituents enhance the solubility of the complexes in organic solvents. 6,6'-Substituents tend to protect the metal center. [8] The related N,N-heterocyclic ligand phenanthroline forms similar complexes.