Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/95386
Title: UPS study of compounds with metal-silicon bonds: M(CO)nSiCl3 (M = Co, Mn; n = 4, 5) and Fe(CO)4(SiCl3)2
Authors: Novak, I. 
Huang, W. 
Luo, L.
Huang, H.H. 
Ang, H.G. 
Zybill, C.E. 
Issue Date: 15-Apr-1997
Citation: Novak, I.,Huang, W.,Luo, L.,Huang, H.H.,Ang, H.G.,Zybill, C.E. (1997-04-15). UPS study of compounds with metal-silicon bonds: M(CO)nSiCl3 (M = Co, Mn; n = 4, 5) and Fe(CO)4(SiCl3)2. Organometallics 16 (8) : 1567-1572. ScholarBank@NUS Repository.
Abstract: The (trichlorosilyl) (and -germyl)metal carbonyls Co(CO)4SiCl3, Co(CO)4GeCl3, Mn(CO)5-SiCl3, and cis-Fe(CO)4(SiCl3)2 have been synthesized in high yields. He I photoelectron spectra (UPS) of the complexes have been measured and interpreted on the basis of empirical arguments and density functional theory (DFT) calculations. For cis/trans-Fe(CO)4(SiCl3)2 isomers the calculations predict the trans-isomer to be more stable than cis by 15.2 kJ mol-1. The cis-isomer is exclusively present in the solid state and in the gas phase. UPS results suggest the importance of charge polarization effects and the lack of π-back-donation along TM-Si bonds. The calculated M-Si bond distances amounted to 2.34 Å (Co-Si), 2.43 Å (Co-Ge), 2.47 Å (Mn-Si), 2.41 Å (trans-Fe-Si), and 2.45 Å (cis-Fe-Si). For Co(CO)4SiCl3, the DFT calculated Co-Si bond dissociation energy was 317.7 kJ mol-1, compared to 222.2 kJ mol-1 for Co-C energy in Co(CO)4CCl3.
Source Title: Organometallics
URI: http://scholarbank.nus.edu.sg/handle/10635/95386
ISSN: 02767333
Appears in Collections:Staff Publications

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