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Autor(en) / Beteiligte
Titel
Reactivity of Transition Metal Gallylene Complexes Toward Substrates with Multiple Carbon–Element Bonds
Ist Teil von
  • Inorganic chemistry, 2022-09, Vol.61 (38), p.14962-14972
Ort / Verlag
American Chemical Society
Erscheinungsjahr
2022
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Reactivity of transition metal complexes containing the redox-active gallylene (dpp-bian)Ga ligand (dpp-bian = 1,2-bis­[(2,6-diisopropylphenyl)­imino]­acenaphthene) toward isocyanide, isocyanate, isothiocyanate, and ketene substrates is described. The reaction of [(dpp-bian)­GaCr­(CO)5] (1) with tBuNC results in a dative complex [(dpp-bian)­Ga­(CNtBu)­Cr­(CO)5] (2), while compound [(dpp-bian)­GaCr­(CO)5]2[Na­(THF)2]2 (3) reacts with tBuNC to give the coordination polymer [(dpp-bian)­GaCr­(CO)5]­[Na­(CNtBu)­(THF)]n (5). Treatment of [(dpp-bian)­GaCr­(CO)5]2[Na­(THF)2]2 with an excess of PhNCO results in trimerization of the latter and formation of complex [(dpp-bian)­GaCr­(CO)5]­[Na­(PhNCO)3(Et2O) (DME)] (4). [(dpp-bian)­GaFeCp­(CO)2] (7) treated with Ph2CCO or PhNCS results in cycloaddition products [(dpp-bian)­(Ph2CCO)­GaFeCp­(CO)2] (8) and [(dpp-bian)­(PhNCS)­GaFeCp­(CO)2] (9). The formation of 2 and 9 was found to be reversible, which offers a means for facile regulation of transition metal center reactivity and cooperative substrate activation. New compounds were characterized by EPR (2), NMR (4, 8, and 9), and IR spectroscopy (2, 4, 5, 8, and 9). The molecular structures of 2, 4, 5, 8, and 9 were established by single-crystal X-ray diffraction analysis. Electronic structures of the compounds have been examined by DFT calculations.
Sprache
Englisch
Identifikatoren
ISSN: 0020-1669
eISSN: 1520-510X
DOI: 10.1021/acs.inorgchem.2c01296
Titel-ID: cdi_proquest_miscellaneous_2714391814
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