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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Reactions of (Ph)tBuP-P(SiMe3)Li center dot 3THF with [(PNP) TiCl2] and [(Me)NacNacTiCl(2)center dot THF]: synthesis of first PNP titanium(IV) complex with the phosphanyl-phosphinidene ligand [(PNP)Ti(Cl){eta(2)-P-P(Ph)tBu}]
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Reactions of (Ph)tBuP-P(SiMe3)Li center dot 3THF with [(PNP) TiCl2] and [(Me)NacNacTiCl(2)center dot THF]: synthesis of first PNP titanium(IV) complex with the phosphanyl-phosphinidene ligand [(PNP)Ti(Cl){eta(2)-P-P(Ph)tBu}]

机译:(pH)TBUP-P(SIME3)Li中心点3THF与[(PNP)TICL2]和[(ME)NACNACTICL(2)中心点THF]:合成第一PNP钛(IV)复合物与磷酰磷烯 配体[(PNP)Ti(CL){ETA(2)-PP(pH)TBU}]

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摘要

Herein, the lithium derivative of diphosphane, (Ph) tBuP-P(SiMe3)Li (1), is isolated for the first time and investigated in reactions with beta-diketiminate ((Me)Nacnac(-) = [Ar]NC(Me)CHC(Me)N[Ar]; Ar = 2,6-iPr(2)C(6)H(3)) and PNP-pincer (PNP = N[2-PiPr(2)-4-methylphenyl](2)) Ti(III) complexes. The beta-diketiminate titanium(III) complex containing the phosphanylphosphido ligand [(Me)NacNacTi(Cl){eta(2)-P(SiMe3)-P(Ph)tBu}] (2) is prepared via the reaction of [(Me)NacNacTiCl(2)center dot THF] with (Ph)tBuP-P(SiMe3)Li in toluene solution with good yield and purity. The corresponding titanium(IV) complex involving the phosphanylphosphinidene ligand [(Me)NacNacTi(Cl){eta(2)-P-P(Ph)tBu}] (3) is synthesized via the oxidation of complex (2) with [iBu(3)PAgCl](4). Interestingly, an analogous PNP titanium(IV) complex, [(PNP) Ti(Cl){eta(2)-P-P(Ph) tBu}] (4), is obtained in the reaction of [(PNP)TiCl2] with (Ph)tBuP-P(SiMe3) Li in toluene solution and a 1 : 1 molar ratio instead of the expected titanium(III) complex with the phosphanylphosphido ligand. The solid-state structures of (Ph)tBuP-P(SiMe3)Li center dot 3THF (1), [(Me)NacNacTi(Cl){eta(2)-P(SiMe3)-P(Ph)tBu}] (2), [(Me)NacNacTi(Cl){eta(2)-P-P(Ph)tBu}] (3) and [(PNP)Ti(Cl){eta(2)-P-P(Ph)tBu}] (4) are determined by single-crystal X-ray diffraction, which reveals that in all obtained complexes, both the phosphanylphosphinidene (Ph)tBuP-P and phosphanylphosphido (Ph)tBuP-P(SiMe3) ligands are bidentate-coordinated to the metal center.
机译:在此,第一次分离二膦,(pH)(pH)TBUP-P(SIME3)Li(1)的锂衍生物,并在用β-二酮酸((ME)NaCNAC( - )= [AR] NC( ME)CHC(ME)N [AR]; AR = 2,6-IPR(2)C(6)H(3))和PNP-iner(PNP = N [2-PIPR(2)-4-甲基苯基] (2))Ti(III)复合物。含有磷酰基磷酰配体[(ME)Nacnacti(Cl){Eta(2)-P(SIME3)-P(PH)TBU}](2)的β-二酮型络合物由[( ME)NaCnacticl(2)中心点THF]用(pH)TBUP-P(SIME3)Li在甲苯溶液中具有良好的产量和纯度。涉及磷酰基氨基丙烯配体[(ME)Nacnacti(Cl){ETA(2)-PP(pH)TBU}](3)的相应钛(IV)复合物通过络合物(2)与[IBU(3 )pagcl](4)。有趣的是,在[(PNP)TiCl2]的反应中,获得了一种类似的PNP钛(IV)复合物[(PNP)Ti(Cl)含量,[(PNP)Ti(Cl){Eta(2)-PP(pH)TBU}](4) pH)TBUP-P(SIME3)Li在甲苯溶液中和1:1摩尔比而不是与磷酸磷酰基磷脂配体的预期钛(III)配合物。 (pH)TBUP-P(SIME3)LI中心点3thf(1),[(ME)Nacnacti(CL){ETA(2)-P(SIME3)-P(PH)TBU}]( 2),[(ME)NaCnacti(CL){ETA(2)-PP(pH)TBU}](3)和[(PNP)TI(CL){ETA(2)-PP(pH)TBU}]( 4)通过单晶X射线衍射确定,其显示在所有得到的络合物中,磷基膦酰基(pH)Tbup-P和磷酸磷酰基 - P(pH)Tbup-P(Sime3)配体都是双齿 - 金属中心的。

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