1986
DOI: 10.1021/ic00236a051
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Ring-substituted derivatives of .eta.5-cyclopentadienyltetracarbonylvanadium: synthesis and vanadium-51 NMR spectroscopic characteristics

Abstract: hexasolventocopper(II) ion in acetic acid is very fast, as expected from the Jahn-Teller effect of the copper(II) ion,2 while the solvent-exchange rate on the copper acetate is much slower, since the latter forms the dimeric structure and the solvated acetic acid molecules at its axial sites are stabilized by hydrogen bonding as depicted in I.Acknowledgment. The present work was supported through a Grant-in-Aid for Scientific Research (No. 59430010) and a Grant-in-Aid for Special Project Research (No. 60129031… Show more

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Cited by 28 publications
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“…The X-ray structures of V(TI 5 -C 5 HS)(CO) 3 The use of PdO as catalyst in a ratio PdO/V=l/5 decreases the reaction time from 4 hours (without PdO) to 10 minutes.…”
Section: Carbonyl and Group V Donor Atom Ligandsmentioning
confidence: 99%
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“…The X-ray structures of V(TI 5 -C 5 HS)(CO) 3 The use of PdO as catalyst in a ratio PdO/V=l/5 decreases the reaction time from 4 hours (without PdO) to 10 minutes.…”
Section: Carbonyl and Group V Donor Atom Ligandsmentioning
confidence: 99%
“…There are two different routes to the THF vanadium complex by photolysis of THF solutions of V(ti 5 -C 5 Chalcogenides complexes of vanadium of general formula V(n 5 -C 5 H 5 )(CO) 3 EMe 2 (E=S,Se,Te), see Table 5, can be prepared by irradiation ofV^5-C 5 H 5 )(CO) 4 in the presence of EMe 2 (E=S,Se,Te) /23/. X-ray structural determination of ν(η 5 -ΰ 5 Η 5 )(03) 3 SMe 2 is shown in section 2.4, Figure 2 The high-field (low-frequency) isotope shift of metal shielding,on conversion of [Υ(η 5 -0 5 Η 5 )(00) 3 Ή]-to [V^5-C s H 5 )(CO) 3 2 H]·, has been studied and the isotope effect is of the order -4,7ppm. /8/.…”
Section: Carbonyl and Group VI Donor Atom Ligandsmentioning
confidence: 99%
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