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...0.1021/ja01582a036|title=Acetylenic Dicobalt Hexacarbonyls. Organometallic Compounds Derived from Alkynes and Dicobalt Octacarbonyl1,2 |year=1956 |last1=Greenfi [[Category:Organocobalt compounds]] ...

'''Cobalt tricarbonyl nitrosyl''' is the [[organocobalt compound]] with the formula Co(CO)₃(NO). It is a dark red volat ...]]:<ref>King, R. B. "Organometallic Synthesis, Volume 1: Transition-metal compounds" (1965) Academic Press. {{ISBN|0124080502}}</ref> ...

==Related compounds== ...sub>2</sub>.<ref>{{cite journal |doi=10.1007/BF00800262 |title=New Type of Organocobalt Complexes Structure of η²-aminomethylenebis(2,2?-bipyridyl) Cob ...

'''Cyclopentadienylcobalt dicarbonyl''' is an [[organocobalt]] compound with formula (C₅H₅)Co(CO)₂, abb ...=[[Wilkinson, G.]] | title = Cyclopentadienyl-carbon monoxide and related compounds of some transitional metals. | journal = [[Journal of Inorganic and Nuclear ...

| journal = Chemistry of Heterocyclic Compounds ...ion, alkynes and nitriles react in the presence of [[organocobalt compound|organocobalt catalysts]], a reaction inspired by [[alkyne trimerization]].<ref name=ul/> ...

'''Decamethylcobaltocene''' is an [[organocobalt compound]] with the formula Co(C₅(CH₃)₅)<s [[Category:Organocobalt compounds]] ...

[[Category:Cobalt(II) compounds]] [[Category:Organocobalt compounds]] ...

...as '''bis(cyclopentadienyl)cobalt(II)''' or even "bis Cp cobalt", is an [[organocobalt compound]] with the formula Co(C₅H₅)₂. It ...to a group of organometallic compounds called [[metallocene]]s or sandwich compounds.<ref>{{cite book|first1=C. |last1=Elschenbroich |first2=A. |last2=Salzer |t ...

...[[acrylonitrile]] and [[acetylene]] below 130–140 ̊C in the presence of [[organocobalt compound]]s as a catalyst.<ref name=Ullmann/> Acrylonitrile is the solvent ...rene]], [[butadiene]], [[isobutylene]], [[methyl methacrylate]], and other compounds in the presence of radical, cationic, or anionic initiators. The homopolyme ...

[[Category:Organocobalt compounds]] ...

...1=J. D. |last2=Beyersmann |first2=D. |year=2005 |chapter=Cobalt and Cobalt Compounds |title=Ullmann's Encyclopedia of Industrial Chemistry |publisher=Wiley-VCH {{Hydrogen compounds}} ...

...llic chemistry]] and [[organic synthesis]], and is central to much known [[organocobalt chemistry]].<ref name = Pauson>{{cite encyclopedia|first1 = Peter L.|last1 ...lmann /><ref name = cyanide>{{cite book|chapter = Hydrogenation of Organic Compounds with Synthesis Gas|first = Milton|last = Orchin|title = Advances in Catalys ...

'''Cobalt compounds''' are [[chemical compounds]] formed by [[cobalt]] with other elements. == Inorganic compounds == ...

| title = Cotrimerizations of Acetylenic Compounds|author1=Agenet, N. |author2=Buisine, O. |author3=Slowinski, F. |author4=Gan ...W. J. Schweckendiek reported their wartime results showing that [[nickel]] compounds are effective catalysts:<ref>{{cite journal|author1=Reppe, W. |author2=Schw ...

[[Category:Organocobalt compounds]] ...

Most commonly applied cobalt compounds are cobaloximes, cobalt [[porphyrin]]s and Co([[Metal acetylacetonates|acac ...t4=Fryd|first4=Michael|title=Living Radical Polymerization of Acrylates by Organocobalt Porphyrin Complexes|journal=Journal of the American Chemical Society|volume ...

...can convert cyanocobalamin to any one of the active vitamin {{chem|B|12}} compounds.{{R|PMC2809139}} ...[[methylcobalamin]], [[hydroxocobalamin]] and [[adenosylcobalamin]]. These compounds are converted to cyanocobalamin by addition of [[potassium cyanide]] in the ...

...ufacture of [[magnetic]], wear-resistant and high-strength [[alloy]]s. The compounds cobalt silicate and [[Cobalt blue|cobalt(II) aluminate]] (CoAl₂O ==Compounds== ...