ChemInform Abstract: TRANSITION METAL METHYLENE COMPLEXES, IV. NOVEL METHYLENE COBALT COMPLEXES

1978 ◽  
Vol 9 (21) ◽  
Author(s):  
W. A. HERRMANN
2018 ◽  
Vol 47 (13) ◽  
pp. 4678-4684 ◽  
Author(s):  
Maykon A. Lemes ◽  
François Magnan ◽  
Bulat Gabidullin ◽  
Jaclyn Brusso

A hexaazatrinaphtylene-based transition metal complex that exhibits single molecule magnet behaviour is reported herein. This study reveals the influence of both nuclearity and topology on the magnetic properties of hexaazatrinaphtylene-based complexes.


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.


1970 ◽  
Vol 23 (3) ◽  
pp. 475 ◽  
Author(s):  
RS Dickson ◽  
PJ Fraser

The new organocobalt complex CO2(CO)4(CF3C2CF3)2(CF3C2H) has been isolated from the reaction of hexafluorobut-2-yne with p-trifluoropropyne-hexacarbonyldicobalt. In addition, a second isomer of the known complex CO2(CO)4(CF3C2CF3)2(CF3C2H)2 has been isolated from the reaction of 3,3,3-tri-fluoropropyne with p-hexafluorobut-2-yne-hexacarbonyldicobalt. A detailed study of the 1H and 19F N.M.R. spectra of these and the related complexes Co2(C0)4- (CF3C2CF3)3 and CO2(CO)4(CF3C2H)3 has led to an assignment of the substituent arrangement in all of these complexes.


1971 ◽  
Vol 49 (16) ◽  
pp. 2726-2732 ◽  
Author(s):  
D. G. Holah ◽  
C. N. Murphy

The synthesis and some properties of ethylxanthate (Xan−) complexes, MXan2 and MXan3− (M = manganese(II) and iron(II)) are reported. Reactions between divalent metal halides (manganese, iron, cobalt, nickel, copper, and zinc) and Xan− and between the metal halides and N,N-diethyldithiocarbamate (dtc−) in the presence of nitrogen bases 1,10-phenanthroline (phen) and 2,2′-bipyridyl (bipy) are described. The major products of these reactions are complexes of the type MXan2.Base and Mdtc2.Base (with notable exceptions). In the former series with bipy, two different crystalline modifications of the manganese, iron, and cobalt complexes are formed, and copper(II) is reduced to copper(I) by Xan− in the presence of both bases. In the nickel–dtc system with bipy, Nidtc2 is produced, while with phen, the complex [Niphen3]dtc2 is formed. The latter reacts very rapidly with methylene chloride. Cudtc2 is produced from the copper(II)/base/dtc reactions.


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