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Carbonyl Complexes Possessing Column Structures

However, these compounds exhibit smaller conductivities compared to non-stoichiometric iridium complexes because the band is completely occupied. Moreover, the overlap of orbitals in those rhodium complexes is less effective than in iridium compounds. [Pg.122]

Wender and P. Pino (eds.), Organic Syntheses via Metal Carbonyls Vol. 1, Interscience, New York (1968). [Pg.122]

Tomilov, I. N. Chernykh, and Yu. M. Kargin, in Elektrokhimia Elementooranicheskich SoyedineniU Nauka, Moscow (1985). [Pg.122]

Balhausen and H. B. Gray, Molecular Orbital Theory, Benjamin, New York (1965). [Pg.122]

Fenske, Abstracts of Papers, XIII ICCC Krakow-Zakopane (Sept. 1970) Pure App. Chem., 27, 61 (1971) M. B. Hall and R. F. Fenske, Inorg. Chem., 11, 1619 (1972). [Pg.122]


Column structures have also been determined for carbonyl complexes of rhodium, iridium, and platinum. For platinum complexes of the formula [Pt3(CO)6] , the maximum value of n probably does not reach more than 20 (Figure 3.26) and therefore these carbonyls do not show anisotropy of conductivity. Various Ir(I) and Rh(I) complexes possessing column structures are known [IrX(CO)3] (X = C1, Br, I), [IrCl,o7(CO)2.93], [Ir(acac(CO)2], Ho.38lrCl2(CO)2(H20)2.9, Ko.58[IrCl2(CO)2], and... [Pg.121]




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Carbonyls structure

Columns complex

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