Thermochemical and spectroscopic properties of transition-metal complexes. Part II. Cobalt complexes of the type CoL2X2(L =o-, m-, or p-fluoroaniline, and X = chlorine, bromine, or iodine)

Author(s):  
G. Beech ◽  
G. Marr ◽  
B. W. Rockett
1968 ◽  
Vol 21 (1) ◽  
pp. 97 ◽  
Author(s):  
RS Dickson ◽  
DBW Yawney

Treatment of pentacarbonyliron with pentafluorophenylacetylene has given the stable complex tricarbonyl-2,5-bis(pentafluorophenyl)cyclopentadienoneiron. There is no evidence of the formation of other structural isomers. The complex is also formed from pentafluorophenylaoetylene and nonacarbonyldiiron or dodecacarbonyltriiron. Two alkyne-cobalt complexes have been isolated from the interaction of octacarbonyldicobalt and pentafluorophenylacetylene. One of these is a bridging alkyne complex of molecular stoicheiometry Co2(CO)6(C6F6CCH); the second is a complex of formula Co3(CO)9(CCH2C6F5). The infrared and nuclear magnetic resonance spectra of the complexes are given, and the probable structures of the compounds are deduced from these spectroscopic properties.


1981 ◽  
Vol 54 (1) ◽  
pp. 163-169 ◽  
Author(s):  
Yukito Murakami ◽  
Yoshihisa Matsuda ◽  
Kazunori Sakata ◽  
Sunao Yamada ◽  
Yasuhiro Tanaka ◽  
...  

1969 ◽  
Vol 22 (3) ◽  
pp. 533 ◽  
Author(s):  
RS Dickson ◽  
DBW Yawney

Two new organocobalt complexes, Co2(CO)4(CF3C2CF3)3 and Co2(CO)4(CF3C3H)2- CF3C2CF3, have been isolated from the appropriate reactions of hexafluorobut-2-yne with octacarbonyldicobalt and of 3,3,3- trifluoropropyne with μ-hexafluorobut-2-yne-hexacarbonyldicobalt. The probable structures of these compounds are discussed in light of their infrared and nuclear magnetic resonance spectra. ��� The direct formation of complexes of the type Co3(CO)9CCH2R has been established in the reactions of several terminal alkynes, RC2H (R = H, CF3, C6H5), with octacarbonyldicobalt. The spectroscopic properties of the products so obtained are given.


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