Titanium(IV) Cations with Trigonal Monopyramidal Geometry: Unusual Lewis Acids Supported by a Triaryl Triamido-Amine Ligand.
Titanium(IV) Cations with Trigonal Monopyramidal Geometry: Unusual Lewis Acids Supported by a Triaryl Triamido-Amine Ligand.
复制标题
具有三角单锥体几何形状的钛(IV)阳离子:三芳基三酰胺胺配体支持的不寻常的路易斯酸
作者:
van Krüchten;Spaniol
Protonolysis of the titanium alkyl complex [Ti(CH2SiMe3)(Xy‐N3N)] (Xy‐N3N=[{(3,5‐Me2C6H3)NCH2CH2}3N]3−) supported by a triamidoamine ligand, with [NEt3H][B(3,5‐Cl2C6H3)4] or [PhNMe2H][B(C6F5)4] afforded the cations [Ti(Xy‐N3N)][A] (A−=[B(3,5‐Cl2C6H3)4]−(1[B(ArCl)4]; B(ArCl)4=tetrakis(3,5‐dichlorophenyl)borate); A−=[B(C6F5)4]−(1[B(ArF)4]; B(ArF)4=tetrakis[3,5‐bis(trifluoromethyl)phenyl]borate). These Lewis acidic cations were reacted with coordinating solvents to afford the cations [Ti(L)(Xy‐N3N)][B(C6F5)4] (2‐L; L=Et2O, pyridine and THF). XRD analysis revealed a trigonal monopyramidal (TMP) geometry for the tetracoordinate cations in1[B(ArX)4]and trigonal bipyramidal (TBP) geometry for the pentacoordinate cations in2‐L. Variable‐temperature NMR spectroscopy showed a dynamic equilibrium for2‐Et2Oin solution, involving the dissociation of Et2O. Coordination to the titanium(IV) center activated the THF molecule, which, in the presence of NEt3, underwent ring‐opening to give the titanium alkoxide [Ti(O(CH2)4NEt3)(Xy‐N3N)][B(3,5‐Cl2C6H3)4] (3). Hydride abstraction from Cβ,eqof the triamidoamine ligand arm in [Ti(CH2SiMe3)(Xy‐N3N)] or [Ti(NMe2)(Xy‐N3N)] with [Ph3C][B(3,5‐Cl2C6H3)4] led to the diamidoamine–imine complex [Ti(R){(Xy‐N=CHCH2)(Xy‐NCH2CH2)2N}][B(3,5‐Cl2C6H3)4] (R=CH2SiMe3(4 a); R=NMe2(4 b)). Hydride addition to4 bwith [Li(THF)][HBPh3] gave [Ti(NMe2)(Xy‐N3N)], whereas KH deprotonated further to give [Ti(NMe2){(Xy‐NCH=CH)(Xy‐NCH2CH2)2N}] (5). XRD on single crystals of3and4 bconfirmed the proposed structures.
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DOI:
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发表时间:
1998
期刊:
影响因子:
--
作者:
P. Roussel;N. Alcock;P. Scott
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P. Scott
DOI:
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发表时间:
2001
期刊:
影响因子:
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DOI:
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发表时间:
1997
期刊:
影响因子:
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R. Schrock
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R. Schrock
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4.6
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C. Hoff
DOI:
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发表时间:
1991
期刊:
影响因子:
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作者:
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