Platinum complexes properties

Tin, nitratodiphenyltris(dimethy) sulfoxide)-structure, 1,77 Tin, nitratotris(triphenyltin)-structure, 1, 47 Tin,tetrakis(acetato)-stereochemistry, 1,94 Tin, tetrakis(diethyldithiocarbamato)-angular parameters, 1, 57 Tin, tetrakis(ethyldithiocarbamato)-angular parameters, 1, 57 Tin, tetranitrato-stereochemistry, 1, 94 Tin, tri-n-butylmethoxy-, 3, 208 Tin alkoxides physical properties, 2, 346 Tin bromide, 3, 194 Tin bromide hydrate, 3,195 Tin carboxylates, 3, 222 mixed valence, 3, 222 Tin chloride, 3, 194 hydroformylation platinum complexes, 6, 263 Tin chloride dihydrate, 3,195 Tin complexes, 3, 183-223 acetyl ace tone... 

A novel chiral dissymmetric chelating Hgand, the non-stabiUzed phosphonium ylide of (R)-BINAP 44, allowed in presence of [Rh(cod)Cl]2 the synthesis of a new type of eight-membered metallacycle, the stable rhodium(I) complex 45, interesting for its potential catalytic properties (Scheme 19) [81]. In contrast to the reactions of stabihzed ylides with cyclooctadienyl palladium or platinum complexes (see Scheme 20), the cyclooctadiene is not attacked by the carbanionic center. Notice that the reactions of ester-stabilized phosphonium ylides of BINAP with rhodium(I) (and also with palladium(II)) complexes lead to the formation of the corresponding chelated compounds but this time with an equilibrium be-... 

The eight-coordinate vanadium complex V(S2CMe)4 contains both dodecahedral and square prismatic eight-coordinate molecules in the same crystal.322 Of particular interest is the chain-like, mixed valence platinum complex [Pt2(S2CMe)4( i-I)]A, which displays unusual electrical properties metallic conduction between 300 and 340 K and semiconducting properties below 300 K,323 whereas the analogous nickel complex, [Ni2(S2CMe)4(p-I)]x is a semiconductor.324... 

Kinetics and mechanisms of substitution at Pt(IV) are occasionally mentioned in relation to those complexes which may have anti-tumor properties. An article on molecular modeling of interactions between platinum complexes and nucleotides or DNA includes a brief mention of Pt(IV) (178). 

The early empirical structure-activity relationships promoted discovery of second-generation anticancer drugs such as complexes 2 and 3. However, analogs of these drugs usually display similar clinical profiles to the parent drugs. Therefore new classes of platinum complexes are required with distinct properties. 

A rich family of intensely blue-coloured, linear platinum complexes, called platinum blues , has received a great body of attention in the years from 1970 to 1990, not only for their unusual physico-chemical properties, but also for their antitumor properties.14... 

Direct Cg cyclization of alkanes into cyclohexane-type rings. The occurrence of this process is claimed under the effect of unreduced surface platinum complexes which have no metallic properties (24). 

Chelate complexes of the type [PdX2(diene)] (X = Cl, Br) are readily formed by the dienes hexa-1,5-diene (124), bicyclo 2,2,lJhepta-2,5-diene (1, 7) tricyclo[4,2,2,0]-deca-triene and -diene derivatives (10), cyclo-octa-1,5-diene and dicyclopentadiene, but not dipentene (43). These may be converted to complexes of the types [Pd2X2(dieneOR)2] and [PdCl(dieneOR)-(amine)] (R = alkyl) (43), and their properties indicate that they have similar structures to the platinum complexes (XXXI) and (XXXIII). 

Platinum complexes (continued) with aryls, thallium adducts, 3, 399 with bis(alkynyl), NLO properties, 12, 125 with bisalkynyl copper complexes, 2, 182-186 with bis(3,5-dichloro-2,4,6-trifluorophenyl), 8, 483 and C-F bond activation, 1, 743 in C-H bond alkenylations, 10, 225 in C-H bond electrophilic activation studies, 1, 707 with chromium, 5, 312 with copper, 2, 168 cyclometallated, for OLEDs, 12, 145 in diyne carbometallations, 10, 351-352 in ene-yne metathesis, 11, 273 in enyne skeletal reorganization, 11, 289 heteronuclear Pt isocyanides, 8, 431 inside metallodendrimers, 12, 400 kinetic studies, 1, 531 on metallodendrimer surfaces, 12, 391 mononuclear Pt(II) isocyanides, 8, 428 mononuclear Pt(0) isocyanides, 8, 424 overview, 8, 405-444 d -cP oxidative addition, PHIP, 1, 436 polynuclear Pt isocyanides, 8, 431 polynuclear Pt(0) isocyanides, 8, 425 Pt(I) isocyanides, 8, 425 Pt(IV) isocyanides, 8, 430... 

The properties of the complex of homoadamantyne, which is formally a cycloheptyne, more closely resemble platinum complexes of cyclohexyne than those of the seven-membered ring alkyne. The bend-back angle (50.6°) (Table VIII) is significantly larger than that of the corresponding cycloheptyne complex (41.3°) and nearly as large as that of the cyclohexyne analogue... 

Very few dithiolene platinum complex-based compounds have been reported and most of them exhibit poor electrical conductivity (9, 122, 123). The complex (Me4N)[Pt(dmit)2]2 does show metal-like behavior (RT conductivity = 10 S cm 1) but only >220 K (123). Another exception is (NHMe3)[Pt(dmit)2]3. This compound, which has the unusual 1 3 stoichiometry, behaves as a metal down to 180 K, with a room temperature conductivity of 140 S cm-1 (91). The Pt(dmit)2 units form pairs with an eclipsed overlap mode. Unlike the analogue Ni derivatives (see above) substituting one hydrogen atom for one methyl group in the (Me4N)+ cation leads to an improvement in the electrical properties. 

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