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水溶性膦。17.(1)具有二磺化1,1'-联苯主链和二苯并膦环戊二烯部分的新型水溶性仲膦和叔膦。

Water-soluble phosphines. 17.(1) novel water-soluble secondary and tertiary phosphines with disulfonated 1,1'-biphenyl backbones and dibenzophosphole moieties.

作者信息

Herd Oliver, Hoff Dietmar, Kottsieper Konstantin W, Liek Christian, Wenz Kirsten, Stelzer Othmar, Sheldrick William S

机构信息

Fachbereich 9, Anorganische Chemie, Bergische Universität Wuppertal, Gaussstrasse 20, D-42097 Wuppertal, Germany.

出版信息

Inorg Chem. 2002 Oct 7;41(20):5034-42. doi: 10.1021/ic011239z.

Abstract

Reaction of 2,2'-difluoro-1,1'-biphenyl with chlorosulfonic acid and subsequent hydrolysis followed by neutralization with potassium or sodium hydroxide affords disodium or dipotassium 5,5'-disulfonato-2,2'-difluoro-1,1'-biphenyl (1a, 1b). On treatment of 1b with diphenyl- or phenylphosphine in the superbasic medium DMSO/KOH, phosphine ligand 2 or 3 with a disulfonated 1,1'-biphenyl backbone or a dibenzophosphole moiety is formed. The structure of the oxide of 5-phenyldibenzophosphole 3, which crystallizes as 4.2.5H(2)O in the monoclinic space group P2(1)/n with a = 13.799(3) A, b = 19.246(4) A, c = 17.764(4) A, beta = 105.63(3) degrees, and Z = 4, has been determined by X-ray analysis. Nucleophilic phosphination of 1a with NaPH(2) in liquid ammonia yields the sodium phosphide 5a which on protonation gives the water-soluble 5H-dibenzophosphole 5. Reaction of 1b with PH(3) in the superbasic medium DMSO/KOtBu affords 5b in addition to the oxidation product 6a. On oxidation of 5a or 5b with H(2)O(2), the sodium or potassium salts of the sulfonated phosphinic acids 6a or 6b, respectively, are formed. Alkylation of the sodium dibenzophospholide 5a with 2,2'-bis(chloromethyl)-1,1'-biphenyl or 1,4-di-O-p-toluenesulfonyl-2,3-O-isopropylidene-D-threitol yields the chiral water-soluble bidentate phosphine ligands 8 and 9, respectively.

摘要

2,2'-二氟-1,1'-联苯与氯磺酸反应,随后水解,再用氢氧化钾或氢氧化钠中和,得到5,5'-二磺酸钠或5,5'-二磺酸二钾盐-2,2'-二氟-1,1'-联苯(1a,1b)。在超碱性介质二甲基亚砜/氢氧化钾中,用二苯基膦或苯基膦处理1b,可形成具有二磺化1,1'-联苯主链或二苯并膦环部分的膦配体2或3。5-苯基二苯并膦环3的氧化物以4·2·5H₂O形式在单斜空间群P2(1)/n中结晶,a = 13.799(3) Å,b = 19.246(4) Å,c = 17.764(4) Å,β = 105.63(3)°,Z = 4,其结构已通过X射线分析确定。在液氨中,1a与NaPH₂进行亲核磷化反应生成磷化钠5a,5a经质子化得到水溶性的5H-二苯并膦环5。在超碱性介质二甲基亚砜/叔丁醇钾中,1b与PH₃反应,除氧化产物6a外,还生成5b。用H₂O₂氧化5a或5b,分别形成磺化次膦酸6a或6b的钠盐或钾盐。二苯并膦环钠5a与2,2'-双(氯甲基)-1,1'-联苯或1,4-二-O-对甲苯磺酰基-2,3-O-异亚丙基-D-苏糖醇烷基化,分别得到手性水溶性双齿膦配体8和9。

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