Cyclooctatetraene complexes of yttrium. and the lanthanides with bis(phosphinimino)methanides: Synthesis, structure, and hydroamination/cyclization catalysis

被引:99
作者
Panda, TK [1 ]
Zulys, A [1 ]
Gainer, MT [1 ]
Roesky, PW [1 ]
机构
[1] Free Univ Berlin, Inst Chem, D-14195 Berlin, Germany
关键词
D O I
10.1021/om0491138
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of cyclooctatetraene bis(phosphinimino)methanide complexes of yttrium and the lanthanides, [{CH(PPh2NSiMe3)(2)}Ln(eta(8)-C8H8)] (Ln = Y, Sm, Er, Yb, Lu), were synthesized via three different pathways. The title compounds can be obtained either from [(eta(8)-C8H8)LnI(THF)(3)] and K{CH(PPh2NSiMe3)(2)} or from K2C8H8 and [{CH(PPh2NSiMe3)(2)}LnCl(2)](2). In a third approach the title compounds were synthesized in a one-pot reaction starting from K{CH(PPh2NSiMe3)(2)}, LnCl(3), and K2C8H8. All complexes have been characterized by crystal X-ray diffraction. The solid-state structures of these complexes show that both ligands completely shield the metal center. As a result of the steric crowding, both ligands are slightly asymmetrically attached to the metal. Even though the title compounds are noncharged lanthanide complexes with no obvious leaving group and no coordinated solvent molecules, the compounds were tested as catalysts for the hydroamination/cyclization reaction. A moderate catalytic activity at elevated temperature is observed.
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页码:2197 / 2202
页数:6
相关论文
共 51 条
[1]   Novel dialkyl aluminum bis(iminophosphorano) methanide and methanediide complexes [J].
Aparna, K ;
McDonald, R ;
Ferguson, M ;
Cavell, RG .
ORGANOMETALLICS, 1999, 18 (21) :4241-4243
[2]   Organolanthanide-catalyzed hydroamination/cyclization. Efficient allene-based transformations for the syntheses of naturally occurring alkaloids [J].
Arredondo, VM ;
Tian, S ;
McDonald, FE ;
Marks, TJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (15) :3633-3639
[3]   Organolanthanide-catalyzed intramolecular hydroamination/cyclization of aminoallenes [J].
Arredondo, VM ;
McDonald, FE ;
Marks, TJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (19) :4871-4872
[4]   Multifunctional behavior by a bis-(phosphinimino)methanide ligand:: η2- vs η3-coordination vs Bronsted basicity [J].
Bibal, C ;
Pink, M ;
Smurnyy, YD ;
Tomaszewski, J ;
Caulton, KG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (08) :2312-2313
[5]  
Bürgstein MR, 2001, CHEM-EUR J, V7, P3078, DOI 10.1002/1521-3765(20010716)7:14<3078::AID-CHEM3078>3.0.CO
[6]  
2-E
[7]   (Aminotroponiminato)yttrium amides as catalysts in alkyne hydroamination [J].
Burgstein, MR ;
Berberich, H ;
Roesky, PW .
ORGANOMETALLICS, 1998, 17 (08) :1452-1454
[8]   Lanthanide complexes derived from (R)-1,1′-binaphthyl-2,2′-bis(neopentylamine) -: {Li(THF)4}{Ln[(R)-C20H12N2(C10H22)]2} (Ln = Sm, Yb) -: novel catalysts for enantioselective intramolecular hydroamination [J].
Collin, J ;
Daran, JC ;
Schulz, E ;
Trifonov, A .
CHEMICAL COMMUNICATIONS, 2003, (24) :3048-3049
[9]   CYCLOPENTADIENYL-FREE ORGANOLANTHANIDE CHEMISTRY [J].
EDELMANN, FT .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (22) :2466-2488
[10]   Synthesis and structural chemistry of non-cyclopentadienyl organolanthanide complexes [J].
Edelmann, FT ;
Freckmann, DMM ;
Schumann, H .
CHEMICAL REVIEWS, 2002, 102 (06) :1851-1896