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G.A. Razuvaev M.N. Bochkarev L.V. Pankratov 《Journal of organometallic chemistry》1983,250(1):135-143
Metallic lithium and dibenzenechromium displace thallium from (Rf3Ge)3HgTl·1.5DME (Rf = C6F5, DME = 1,2-dimethoxyethane) to give (Rf3Ge)3HgLi·3DME and [(Rf3Ge)4Hg][Cr(C6H6)2]2, respectively. Reactions of thallium germylmercurate with halides of metals and organometallics in DME/EtOH solution produce ionic compounds of [(Rf3Ge)3Hg]? M+ type, which (depending on “M”) (a) may be isolated as pure compounds, (b) disproportionate, (c) form covalent derivatives Rf3Ge-m or (d) undergo alcoholysis. A general scheme for the reactions has been proposed. 相似文献
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[reaction: see text] Trefoil-shaped tris(hexadehydrotribenzo[12]annulene) possessing a substructure of the ultimate two-dimensional C(sp)-C(sp(2)) network, graphyne, and the related tris(tetradehydrotribenzo[12]annulene) were synthesized, and their ground- and excited-state properties were investigated. 相似文献
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G. S. Kalinina E. A. Shchupak N. S. Vyazankin G. A. Razuvaev 《Russian Chemical Bulletin》1976,25(6):1289-1292
1. | Tris[tris(trimethylsilylmethyl)stannyl]- and tris[tris(trimethylsilylmethyl)germyl] thallium, the first stable compounds containing Sn-Tl and Ge-Tl bonds, have been prepared by the reaction of the hydrides of tris (trimethylsilylmethyl)tin and tris (trimethylsilylmethyl)germanium with triethylthallium. |
2. | The Sn-Tl bond is attacked in the reactions of the stannylthallium compound with lithium, mercury, oxygen, bromine, ethyl bromide, ethanol, and other reagents. |
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Edward E. Flagg Donald L. Schmidt 《Journal of polymer science. Part A, Polymer chemistry》1972,10(11):3429-3446
A series of coordination polymers, poly[bis(phosphinatoalanyl)phosphonates], [X(Y)AlOP(R)(O)OAl(Y′)(X′)]n, were synthesized in which the terminal alanyl substituents (X,Y,X,′Y′) consisted of phosphinato (OPRR′O) or fluoro (F) moieties. The properties of the polymers were primarily dependent upon the type of terminal substituent and the hydrocarbon moieties (R,R′) on phosphorus. Polymers with four phosphinato moieties gave molecular weights M?n to 120000 with intrinsic viscosities [η] from 1.5 to 18; the corresponding solids were partially crystalline, melted before decomposition, and were film-forming when larger phosphorus substituents were incorporated. Sequential replacement of the phosphinato moieties with fluorine resulted in molecular weights below 10000 and low viscosities. The properties of the polymers are examined, and the roles of substituents on probable structures are discussed. 相似文献
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Tris(trimethylsilyl)methyllithium reacts with the anhydrous halides MC12 (M = Zn or Cd) to give the compounds [(Me3Si)3C]2M, which show high thermal and chemical stability. They decompose only above 300°C, with formation of (Me3Si)3CH, and are not attacked by water in refluxing THF. The zinc compound can be steam-distilled without decomposition, and does not react with boiling concentrated hydrochloric acid or with bromine in carbon tetrachloride. 相似文献
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The reaction of tris(trimethylsilyl)methylboron dihalides (Me3Si)3CBX2 (X = Cl, F) with the lithium phosphides LiPHtBu and LiPHmes leads to the phosphinoboranes (Me3Si)3CBX‐(PHR), (Me3Si)3CB(PHR)2 or the 1,3,2,4‐diphosphadiboretanes [(Me3Si)3CB(PR)]2, depending on the ratio of the reagents, the reaction temperature and concentration. High dilution and low temperatures are required for the synthesis of (Me3Si)3CB(Hal)PHR ( 1–3 ) in order to prevent the formation of (Me3Si)3CB(PHR)2 ( 4 and 5 ). The latter compounds are best prepared in a two step phosphination from (Me3Si)3CBHal2 and LiPHR. At higher temperatures the four‐membered 1,3,2,4‐diphosphadiboretanes [(Me3Si)3CB(PR)]2 6 and 7 are the most stable compounds. On the other hand, compounds of type (Me3Si)3CB(Hal)PR2, 8 and 9 , are thermally more stable than the monophosphinoboranes 1 – 3 . Phosphinoboranes of type (Me3Si)3CB(PR2)2 (R = tBu, mes) could not be prepared. NMR and mass spectral data are in accord with the monomeric nature of compounds 1 to 9 . 相似文献
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