1981
DOI: 10.1139/v81-181
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Metal derivatives of azoles. Part VII. Gold(I) derivatives of pyrazoles

Abstract: Introduction During our investigation in the field of pyrazolel complexes and of pyrazolates, several gold derivatives of the pyrazolato anion were obtained, including the tri-, di-, and mononuclear species A, B, and C, where the ligand is either bi-or monodentate (I). The first type of compound, A, was obtained, inter alia , through reaction [I]

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Cited by 26 publications
(4 citation statements)
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“…1 Amongst them, the hydrido complexes constitute a large family, with diversified structural and spectroscopic features. [2][3][4] The Pt atoms are often linked through metal-metal bonding and/or hydrido bridges. A bridging hydride may also be associated with another, chemically different bridging unit.…”
Section: Introductionmentioning
confidence: 99%
“…1 Amongst them, the hydrido complexes constitute a large family, with diversified structural and spectroscopic features. [2][3][4] The Pt atoms are often linked through metal-metal bonding and/or hydrido bridges. A bridging hydride may also be associated with another, chemically different bridging unit.…”
Section: Introductionmentioning
confidence: 99%
“…The suggestion that pyrazole and 3,5-dimethylpyrazole form stable hydrogen-bonded trimers (Anderson, Duncan & Rossotti, 1961) gave birth to the idea that replacing the bridging hydrogens with two-coordinate metal atoms would generate trimeric metallocyclic complexes. This idea was successfully explored (Bonati, Minghetti & Banditelli, 1974) and several complexes of the general formula [Au(~-3,5-R2pz)]3 were prepared (Banditelli, Bandini, Minghetti & Bonati, 1981;Banditelli, Bandini, Bonati, Goel & Minghetti, 1982). In the case of R = CF3, a crystallographic study confirmed the expected trimeric structure (Bovio, Bonati & Banditelli, 1984).…”
Section: Introduction Pyrazolato Anions Of the Type 35-r2pzmentioning
confidence: 99%
“…Three phosphine resonances were also present in the 31 P NMR spectrum: d 1 23.63 ppm, d, J P;P ¼ 33.1 Hz, J P;P ¼ 2.5 Hz; 2 J Pt;P ¼ 488 Hz, 1 J Pt;P ¼ 4705 Hz; d 2 3.40 ppm, J P;P ¼ 24.2 Hz, J P;P ¼ 2.5 Hz, 2 J Pt;P ¼ 96 Hz, 1 J Pt;P ¼ 2458 Hz; d 3 1.95, J P;P ¼ 24.2 Hz, J P;P ¼ 33.1 Hz, 2 J Pt;P ¼ 120 Hz, 1 J Pt;P ¼ 2411 Hz ( 2 J Pt;P values are generally considerably smaller than 1 J Pt;P values [45]). These data indicate that a bridging phosphido group is not present as such groups resonate far downfield (>100 ppm) [46].…”
Section: Reactions Of Tetrakis(triethylphosphine)platinum(0) Resultinmentioning
confidence: 92%