Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Angelo J. Amoroso"'
The synthesis of two thiosemicarbazone derivatised ligands (L1 and L2) was accomplished via the reaction of 1-(2-pyridinyl)ethanone hydrazone and either benzoyl or pivaloyl isothiocyanate. A range of Ni(II), Cu(II) and Zn(II) mononuclear complexes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c95d60e9f08c19aaff47d494ec40e34a
https://orca.cardiff.ac.uk/id/eprint/152290/1/1-s2.0-S0277538722004314-main.pdf
https://orca.cardiff.ac.uk/id/eprint/152290/1/1-s2.0-S0277538722004314-main.pdf
Autor:
Ali A. A. Al-Riyahee, Peter N. Horton, Simon J. Coles, Colin Berry, Paul D. Horrocks, Simon J. A. Pope, Angelo J. Amoroso
The synthesis of six N,N′-substituted thiourea ligands (L1a–L3b) was achieved in two steps. A corresponding extensive series of Cu(I), Cu(II), Ni(II) and Zn(II) complexes (1–24) with varying formulations were synthesised from these ligands by t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42f01f773244da7adfccb02a031c09b4
Autor:
M. Carmen Ramírez de Arellano, Paul R. Raithby, Angelo J. Amoroso, Brian F. G. Johnson, Chi Keung Li, Wing Tak Wong, Jack Lewis, Gregory P. Shields
Publikováno v:
Inorganica Chimica Acta. 359:3589-3595
Reactions between the activated cluster [Os 3 (CO) 10 (NCMe) 2 ] and malonic acid, succinic acid and dicarboxylic acetylene, respectively, lead to the formation of the linked cluster complexes [{Os 3 H(CO) 10 } 2 (CO 2 CH 2 CO 2 )] ( 1 ), [{Os 3 H(CO
Publikováno v:
Journal of Chemical Theory and Computation. 2:354-363
Hartree-Fock, density functional, and MP2 methods are applied to the problem of designing neutral, bicyclic C3-symmetric cages incorporating interacting anion- and cation-binding sites which strongly bind NaCl as an ion contact pair. A large number o
Autor:
Lionel P. Clarke, Gregory P. Shields, John E. Davies, Harold R. Powell, Jack Lewis, Angelo J. Amoroso, Paul R. Raithby
Publikováno v:
Journal of Organometallic Chemistry. 635:119-131
The reaction between [Os3(CO)10(NCMe)2] and MeC2C2Me yields the known cluster [Os3(CO)9(μ-CO)(μ3-η2-MeC2C2Me)] (1) and three previously uncharacterised products [Os3(CO)9(μ-CO){μ3-η2:μ3-η1:η1:η3-MeC2C2MeOC5Me2)Os3(μ-CO)(CO)9] (2), [Os3(CO)
Publikováno v:
Organometallics. 20:1115-1127
The racemic methyl complexes (η5-C5Me5)Re(NO)(PR3)(CH3) (R: b, 4-C6H4CH3; c, 4-C6H4-t-C4H9; d, 4-C6H4C6H5; e, c-C6H11), which feature phosphines that are more electron rich and/or bulkier than P(C6H5)3, are elaborated by reactions with HBF4·OEt2/ch
Autor:
Jean Le Bras, Monika Jaeger, Wayne E. Meyer, John A. Gladysz, Wing Tak Wong, Angelo J. Amoroso
Publikováno v:
Journal of Organometallic Chemistry. 616:44-53
Reactions of racemic [(η5-C5Me5)Re(NO)(NCCH3)(CO)]+ BF4− and phosphines PR3 (R=C6H5 a; 4-C6H4CH3 b; 4-C6H4-t-C4H9 c; 4-C6H4C6H5 d; 4-C6H4OCH3 e; c-C6H11 f) give the phosphine carbonyl complexes [(η5-C5Me5)Re(NO)(PR3)(CO)]+ BF4− (5a–5f+ BF4−
Autor:
Paul R. Raithby, Chi Keung Li, Jack Lewis, Angelo J. Amoroso, M. Carmen Ramírez de Arellano, Michael A. Beswick
Publikováno v:
Journal of Organometallic Chemistry. 573:247-253
Treatment of [Os 4 H 4 (CO) 11 ] 2− , [Os 10 C(CO) 24 ] 2− and [Ru 10 C(CO) 24 ] 2− with [Au 2 (Ph 2 PCH 2 PPh 2 )Cl 2 ] in the presence of an excess of TIPF 6 , gave [Os 4 H 4 (CO) 11 (Au 2 Ph 2 PCH 2 PPh 2 )] 1 , [Os 10 C(CO) 24 (Au 2 Ph 2 PC
Autor:
Ward, Angelo J. Amoroso, Jon A. McCleverty, John C. Jeffery, Peter L. Jones, Leigh H. Rees, Elefteria Psillakis
Publikováno v:
Inorganic Chemistry. 36:10-18
Summarization: The hexadentate N6-donor podand tris[3-(2-pyridyl)pyrazolyl]hydroborate (TpPy) contains 2-pyridyl fragments attached to the pyrazolyl C3-positions such that each arm is a bidentate chelate. Three series of lanthanide(III) complexes wer
Autor:
Atta M. Arif, J. A. Gladysz, Weiqing Weng, Marlis Böhme, Jeffery W. Seyler, Yuanlin Zhou, Monika Brady, Angelo J. Amoroso, Gernot Frenking
Publikováno v:
Journal of the American Chemical Society. 119:775-788
Reaction of (η5-C5Me5)Re(NO)(PPh3)(C⋮CH) and Cu(OAc)2 (1.5 equiv, 80 °C, pyridine) gives the orange-brown ReC4Re complex (η5-C5Me5)Re(NO)(PPh3)(C⋮CC⋮C)(Ph3P)(ON)Re(η5-C5Me5) (2, 88%) as a 50:50 diastereomer mixture. Crystallization affords