Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Bruno Longato"'
Publikováno v:
Inorganica Chimica Acta. 361:2985-2988
The 1:1 adduct formed from cis-[(PMePh2)2Pt(NO3)2] and 2,5-bis(4-pyridyl)-1,3,4-thiadiazole (bpytdz) in chloroform crystallizes out as a 1D coordination polymer built up of cis-(PMePh2)2Pt units connected by the bpytdz ligand, an unusual self-assembl
Autor:
Diego Montagner, Bruno Longato
Publikováno v:
Inorganica Chimica Acta. 361:1676-1680
Reaction between the binuclear hydroxo complex cis-[(PPh3)2Pt(μ-OH)]2X2 (X− = NO3, 1a; PF 6 - , 1b) and the model DNA base 9-methyladenine (9-MeAd) leads to the formation of the mononuclear species cis-[(PPh3)2Pt{9-MeAd(-H),N6N7}]X (X− = NO3, 2a
Publikováno v:
Inorganic Chemistry. 45:1805-1814
The hydroxo complex cis-[L2Pt(mu-OH)]2(NO3)2, (L = PMePh2, 1a), in CH3CN solution, deprotonates the NH2 group of 9-methyladenine (9-MeAd) to give the cyclic trinuclear species cis-[L2Pt[9-MeAd(-H)]]3(NO3)3, (L = PMePh2, 2a), in which the nucleobase b
Publikováno v:
European Journal of Inorganic Chemistry. 2004:1092-1099
The dinuclear hydroxo complexes cis-[L2Pt(μ-OH)]2(NO3)2 (L = PMe2Ph and PMePh2) have been characterized by single-crystal X-ray analysis, and their reactivity towards chloride ions has been investigated. Reaction of cis-[L2Pt(μ-OH)]2X2 (L = PMe3, P
Publikováno v:
Inorganic Chemistry. 42:7861-7871
The dinuclear hydroxo complex cis-[L(2)Pt(mu-OH)](2)(NO(3))(2) (L = PMePh(2), 1), in CH(2)Cl(2), CH(3)CN, or DMF solution, deprotonates the NH(2) group of 9-methyladenine (9-MeAd) to give the complex cis-[L(2)Pt[9-MeAd(-H)]](3)(NO(3))(3), 2, which wa
Publikováno v:
European Journal of Inorganic Chemistry. 2003:128-137
Treatment of 9-methyladenine (9-MeAd) with cis-[PtL2(NO3)2] (1) (L = PMe2Ph) in a 2:1 molar ratio generated the bis(adduct) cis-[PtL2(9-MeAd)2](NO3)2 (2), which was isolated and fully characterized by multinuclear (1H, 31P, 13C, 195Pt and 15N) NMR an
Publikováno v:
European Journal of Inorganic Chemistry. 2001:3021-3029
Autor:
Antonio Toffoletti, Roberto Coppo, Giuseppe Pilloni, Giuliano Bandoli, Carlo Corvaja, Bruno Longato
Publikováno v:
Journal of Organometallic Chemistry. :710-718
The rhodium(I) complex stabilised by the organometallic ligand 1,1′-bis(diphenylphosphino)ferrocene (dppf), [Rh(dppf) 2 ] + ( 1 ) can be electrochemically reduced to the Rh(0) and Rh(−1) species, [Rh(dppf) 2 ] ( 2 ) and [Rh(dppf) 2 ] − ( 3 ), r
Publikováno v:
Inorganica Chimica Acta. 277:163-170
Reaction of [Cu(MeCN)4]BF4 with the phosphine Fe[η5-C5H4PPh2]2 (dppf) and its disulfide (dppfS2) sequentially in chlorinated solvents led to the dinuclear tricoordinate complex [{Cu(dppf-P,P′)}2(μ-dppfS2-S,S′)] (BF4)2 (1), whereas reaction of t
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :819-826
The phosphine chalcogenides Fe[η-C 5 H 4 P(E)Ph 2 ] 2 (L) [E = nothing (dppf), S (dptpf) or Se (dpspf)] reacted readily with [Cu(MeCN) 4 ]X (X = BF 4 , PF 6 or ClO 4 ) in CH 2 Cl 2 to give quantitatively the monomeric two-co-ordinated complexes [CuL