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  2. Organometallic chemistry - Wikipedia

    en.wikipedia.org/wiki/Organometallic_chemistry

    A steel bottle containing MgCp 2 (magnesium bis-cyclopentadienyl), which, like several other organometallic compounds, is pyrophoric in air.. Organometallic compounds are distinguished by the prefix "organo-" (e.g., organopalladium compounds), and include all compounds which contain a bond between a metal atom and a carbon atom of an organyl group. [2]

  3. Main group organometallic chemistry - Wikipedia

    en.wikipedia.org/wiki/Main_group_organometallic...

    Main group organometallic chemistry concerns the preparation and properties of main-group elements directly bonded to carbon. The inventory is large. The inventory is large. The compounds exhibit a wide range of properties, including ones that are water-stable and others that are pyrophoric . [ 1 ]

  4. Organozirconium and organohafnium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organozirconium_and_organo...

    Organozirconium chemistry is the science of exploring the properties, structure, and reactivity of organozirconium compounds, which are organometallic compounds containing chemical bonds between carbon and zirconium. [2] Organozirconium compounds have been widely studied, in part because they are useful catalysts in Ziegler-Natta polymerization.

  5. Isolobal principle - Wikipedia

    en.wikipedia.org/wiki/Isolobal_principle

    The isolobal analogy can also be used with isoelectronic fragments having the same coordination number, which allows charged species to be considered. For example, Re(CO) 5 is isolobal with CH 3 and therefore, [Ru(CO) 5] + and [Mo(CO) 5] − are also isolobal with CH 3. Any 17-electron metal complex would be isolobal in this example.

  6. Tolman's rule - Wikipedia

    en.wikipedia.org/wiki/Tolman's_rule

    Many examples of homogeneous catalysis involving organometallic complexes involve shuttling of complexes between 16- and 18-electron configurations. 16-electron complexes often form adducts with Lewis bases and, if low-valent, undergo oxidative addition. CH 3 I + cis-[Rh(CO) 2 I 2] − → [(CH 3)Rh(CO) 2 I 3] −

  7. 18-electron rule - Wikipedia

    en.wikipedia.org/wiki/18-electron_rule

    The most famous example is Vaska's complex (IrCl(CO)(PPh 3) 2), [PtCl 4] 2−, and Zeise's salt [PtCl 3 (η 2-C 2 H 4)] −. In such complexes, the d z 2 orbital is doubly occupied and nonbonding. Many catalytic cycles operate via complexes that alternate between 18-electron and square-planar 16-electron configurations.

  8. Organonickel chemistry - Wikipedia

    en.wikipedia.org/wiki/Organonickel_chemistry

    Organonickel chemistry is a branch of organometallic chemistry that deals with organic compounds featuring nickel-carbon bonds. [1] [2] They are used as a catalyst, as a building block in organic chemistry and in chemical vapor deposition. Organonickel compounds are also short-lived intermediates in organic reactions.

  9. Group 2 organometallic chemistry - Wikipedia

    en.wikipedia.org/wiki/Group_2_organometallic...

    Group 2 organometallic chemistry refers to the organic derivativess of any group 2 element. It is a subtheme to main group organometallic chemistry . [ 2 ] [ 3 ] By far the most common group 2 organometallic compounds are the magnesium-containing Grignard reagents which are widely used in organic chemistry .