A simple molecular orbital model for infrared intensities in metal carbonyl compounds
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference23 articles.
1. Vibrational Spectra and Bonding in Metal Carbonyls. I. Infrared Spectra of Phosphine-substituted Group VI Carbonyls in the CO Stretching Region
2. Spectroscopic studies on organometallic compounds. Part XI. Infrared spectra of pentacarbonyl complexes of metals of the chromium and manganese sub-groups in the carbonyl stretching region
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Infrared and Raman spectra of (η6-C6H6−nXn)Cr(CO)3 complexes where X = Me (n = 0–6) or OMe (n = 0–2). A study of metal—ligand interactions;Journal of Molecular Structure;1994-07
2. Cyclopentadienyl iron xanthate complexes. Crystal and molecular structure and electrochemical reduction of η-C5R5Fe(CO)2(η1-SC(S)OEt) (RH or CH3);Inorganica Chimica Acta;1988-03
3. Absolute integrated infrared intensities of the carbonyl, thiocarbonyl, and selenocarbonyl stretching modes in the chalcocarbonyl complexes Cr(CO)5(CX) and (.eta.6-C6H6)Cr(CO)2(CX) (X = O, S, Se);Organometallics;1984-12
4. Infrared intensity and the co-metal bond;Chemical Physics Letters;1981-01
5. Oxygen-17 n.m.r. shifts of some tungsten carbonyl complexes. A sensitive measure of the σ-donor/π-acceptor ratio of ligands;J. Chem. Soc., Chem. Commun.;1979
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