Genre
- Journal Article
Dimethylplatinum(II) complexes [PtMe2(NN)] {NN = bpy (2,2'-bipyridine), phen (1,10-phenanthroline) or bu2bpy (4,4'-di-tert-butyl-2,2'-bipyridine)} were reacted with alkyl halides (RX = EtI or EtBr, NN = bu2bpy; RX = nBuBr, NN = bpy; RX = CHPh2Br, NN = bpy, phen, or bu2bpy) to yield the Pt(IV) complexes [PtMe2RX(NN)]. On the basis of NMR data, the Pt(IV) product of each reaction contains almost exclusively the kinetic trans isomer, and only in a few cases, very small traces of the thermodn. cis isomers are obsd. The binuclear complexes [Pt2Me4Br2{μ-(CH2)2}(NN)2] (NN = bpy, phen) were obtained from reaction of [PtMe2(NN)] with 1,2-dibromoethane. Notably, the mononuclear complex fac-[PtMe3Br(bpy)], obtained as a byproduct during the reaction of [PtMe2(bpy)] with 1,2-dibromoethane, was characterized by x-ray crystallog. from the reaction of [PtMe2(bpy)] with 1,2-dibromoethane. On the other hand, the reaction of [PtMe2(bu2bpy)] with 1,2-dibromoethane resulted in formation of the mononuclear complex trans-[PtMe2Br{(CH2)2Br}(bu2bpy)]. The reaction of [PtMe2(NN)] with 1,2-bis(dibromomethyl)xylene in a 1:1 or 2:1 mol ratio afforded the mononuclear complexes [PtMe2(CHBr-o-C6H4CHBr2)Br(NN)] (NN = bpy, phen, or bu2bpy) or binuclear complexes [Pt2Me4Br2{μ-o-(CHBr)2C6H4}(NN)2] (NN = bpy, or phen), resp. Finally, 1,3-dibromobutane was oxidatively added to the organoplatinum(II) complexes [PtR2(NN)] (R 2 = (CH2)4, NN = bpy, or phen; R = Me; NN = bpy) via an SN2 mechanism from the less sterically hindered C-Br side to yield the complexes trans-[PtR2Br{(CH2)2CHBrCH3}(NN)]. The products were fully characterized by 1H and 13C NMR spectroscopy and elemental anal. The platinacycle complex [Pt(CH2)4(bpy)] was shown to react faster, as compared to the di-Me analog complex [PtMe2(bpy)], by a factor of 3.8-4.2. The reactions of [Pt(CH2)4(bpy)] or [Pt(CH2)4(phen)] with 1,3-dibromobutane were faster as compared to those with 1,4-dibromobutane, due to the activation effect of the platinum. [on SciFinder(R)]
Department of Chemistry, K.N. Toosi University of Technology, Tehran, Iran.
Copyright (C) 2012 American Chemical Society (ACS). All Rights Reserved.; Section Code: 29-13; CA Section Cross-references: 22, 75; CODEN: JORCAI; CAS Registry Numbers: 38194-04-6P Role: PRP (Properties), SPN (Synthetic preparation), PREP (Preparation) (crystal structure; oxidative addn. of some mono, di or tetra haloalkanes to organoplatinum complexes); 74-96-4 (Ethyl bromide); 75-03-6 (Ethyl iodide); 106-93-4 (1,2-Dibromoethane); 107-80-2 (1,3-Dibromobutane); 109-65-9 (Butyl bromide); 776-74-9 (Bromodiphenylmethane); 13209-15-9 (1,2-Bis(dibromomethyl)benzene); 52594-52-2; 52594-55-5; 68079-67-4; 151111-79-4; 221907-30-8 Role: RCT (Reactant), RACT (Reactant or reagent) (oxidative addn. of some mono, di or tetra haloalkanes to organoplatinum complexes); 96913-51-8P; 1359769-56-4P; 1359769-57-5P; 1359769-58-6P; 1359769-59-7P; 1359769-60-0P; 1359769-61-1P; 1359769-62-2P; 1359769-63-3P; 1359769-64-4P; 1359769-65-5P; 1359769-66-6P; 1359769-67-7P; 1359769-68-8P; 1359769-69-9P; 1359884-74-4P; 1359884-75-5P Role: SPN (Synthetic preparation), PREP (Preparation) (oxidative addn. of some mono, di or tetra haloalkanes to organoplatinum complexes)
Source type: Electronic(1)
Language
- English
Subjects
- structure
- tetra
- Addition reaction kinetics (coordinative, oxidative
- Alkanes Role: RCT (Reactant), RACT (Reactant or reagent) (halo
- addn
- di
- Addition reaction (oxidative
- Steric hindrance (oxidative addn. of some mono, di or tetra haloalkanes to organoplatinum complexes)
- mol
- crystal
- crystal structure
- Kinetics
- oxidative addn. of some mono, di or tetra haloalkanes to organoplatinum complexes)
- trimethyl
- bipyridine
- platinum
- Reaction mechanism
- complex
- organoplatinum
- Molecular structure (of tri-Me platinum bipyridine bromide complex)
- mono
- BROMIDE
- oxidative
- haloalkane