Infrared spectroscopic studies on metal carbonyl compounds. Part XVII. A comparative study of the vibrational spectrum of ditechnetium decacarbonyl and of the decacarbonyls of manganese and rhenium in the C–O stretching region

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Abstract
The i.r. spectra of the M2(CO)10 carbonyls (M = Mn, Tc, or Re) have been reinvestigated in the C–O stretching region with special emphasis on the weak isotopic bands. In the case of the Mn compound the effects of isotopic enrichment have also been examined. The i.r.-inactive (A1, E2, and E3) fundamentals were calculated from the isotopic satellites and the results agree within ±1 cm–1 with recent Raman data. For the technetium compound no Raman study seems to exist and thus the A1(2123 and 1999·5 cm–1), E2(2029 cm–1), and E3(1990·5 cm–1) frequencies reported here are the first data on these i.r.-inactive modes. The force and interaction constants of all three decacarbonyls have been calculated in a C–O factored force field without a priori neglections. Both the equatorial and the axial C–O force constants of Tc2(CO)10[16·642 and 16·316 mdyn Å–1, respectively (1 mdyn Å–1= 102 N m–1)], are the highest in the triad, whereas most of its interaction constants have intermediate values between those of Mn2(CO)10 and Re2(CO)10. For Re2(CO)10 the effect of the eclipsed configuration (D4h) on the eq ⋯ eq′ interaction constants has also been studied.

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