The synthesis, coordination chemistry and ethylene polymerisation activity of ferrocenediyl nitrogen-substituted ligands and their metal complexes

被引:37
作者
Gibson, VC
Gregson, CKA
Halliwell, CM
Long, NJ
Oxford, PJ
White, AJP
Williams, DJ
机构
[1] Univ London Imperial Coll Sci & Technol, London SW7 2AZ, England
[2] Natl Phys Lab, Teddington TW11 0LW, Middx, England
关键词
ferrocene; catalysis; N-ligands; transition metals; ethylene polymerisation;
D O I
10.1016/j.jorganchem.2005.05.051
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Treatment of aminoferrocene with substituted 2-hydroxybenzaldehydes yields the air- and moisture-stable ligands 1-4, which were then reacted to form the chromium dichloride complexes 5-7 and the nickel bis-chelate species 8 and 9. The metal compounds are very air-sensitive but the chromium compounds act as pre-catalysts for the polymerisation of ethylene. Reaction of 1,1'-bis(amino)ferrocene with similarly substituted 2-hydroxybenzaldehyes or simple benzaldehyde gives the ligands 10-12 and 17, respectively. The X-ray crystal structure of 11 shows the molecule to have non-crystallographic C-2 symmetry and to be linked by C-H-...pi interactions between the anthracene rings. Titanium-containing complexes 13-16 can be formed utilising ligands 10-12 and there is a change in geometry within the complexes dependent on the adjacent co-ligands, whilst ligand 17 can be reacted with PdClMe(COD) to form the chelate complex 18. Cyclic voltammetric studies have been carried out on 18 and its oxidised analogue 19, but both complexes are inactive towards ethylene polymerisation. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:6271 / 6283
页数:13
相关论文
共 60 条
[1]   PREPARATION AND CRYSTAL-STRUCTURES OF (1,1'-RUTHENOCENEDITHIOLATO-S,S',RU)(TRIPHENYLPHOSPHINE)-NICKEL(II) AND (1,1'-METALLOCENEDIOXALATO-O,O',FE(OR RU))(TRIPHENYLPHOSPHINE)PALLADIUM(II) - THE METAL (FE OR RU)-METAL (PD OR NI) DATIVE BOND [J].
AKABORI, S ;
KUMAGAI, T ;
SHIRAHIGE, T ;
SATO, S ;
KAWAZOE, K ;
TAMURA, C ;
SATO, M .
ORGANOMETALLICS, 1987, 6 (10) :2105-2109
[2]   STRUCTURE OF A BINUCLEAR [(1R,2R)-N,N'-DISALICYLIDENE-1,2-CYCLOHEXANEDIAMINE]TITANIUM(IV) COMPLEX [J].
AOYAMA, T ;
OHBA, S ;
SAITO, Y ;
SASAKI, C ;
KOJIMA, M ;
FUJITA, J ;
NAKAJIMA, K .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1988, 44 :1309-1311
[3]   The asymmetric addition of trimethylsilyl cyanide to aldehydes catalyzed by chiral (salen)titanium complexes [J].
Belokon, YN ;
Caveda-Cepas, S ;
Green, B ;
Ikonnikov, NS ;
Krustalev, VN ;
Larichev, VS ;
Moscalenko, MA ;
North, M ;
Orizu, C ;
Tararov, VI ;
Tasinazzo, M ;
Timofeeva, GI ;
Yashkina, LV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (16) :3968-3973
[4]   Controlled polymerization of DL-lactide using a Schiff's base al-alkoxide initiator derived from 2-hydroxyacetophenone [J].
Bhaw-Luximon, A ;
Jhurry, D ;
Spassky, N .
POLYMER BULLETIN, 2000, 44 (01) :31-38
[5]   MOLECULAR AND ELECTRONIC-STRUCTURE OF THE COMPLEXES FORMED BY THE SCHIFF-BASE N-(O-HYDROXYBENZYLIDENE)FERROCENEAMINE WITH COII, NIII, CUII, AND ZNII [J].
BRACCI, M ;
ERCOLANI, C ;
FLORIS, B ;
BASSETTI, M ;
CHIESIVILLA, A ;
GUASTINI, C .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1990, (04) :1357-1363
[6]   Synthesis and structural studies of 1,1′-bis-amino-functionalized ferrocenes, ferrocene salts, and ferrocenium salts [J].
Bradley, S ;
Camm, KD ;
Liu, XM ;
McGowan, PC ;
Mumtaz, R ;
Oughton, KA ;
Podesta, TJ ;
Thornton-Pett, M .
INORGANIC CHEMISTRY, 2002, 41 (04) :715-726
[7]   Facile synthesis of amino-functionalised ferrocenes and vanadocenes [J].
Bradley, S ;
McGowan, PC ;
Oughton, KA ;
Thornton-Pett, M ;
Walsh, ME .
CHEMICAL COMMUNICATIONS, 1999, (01) :77-78
[8]   [(3,5-(CF3)2C6H3)4B]-[H(OET2)2]+ - A CONVENIENT REAGENT FOR GENERATION AND STABILIZATION OF CATIONIC, HIGHLY ELECTROPHILIC ORGANOMETALLIC COMPLEXES [J].
BROOKHART, M ;
GRANT, B ;
VOLPE, AF .
ORGANOMETALLICS, 1992, 11 (11) :3920-3922
[9]  
BUTLER IR, 1997, J ORGANOMET CHEM, V552, P53
[10]  
Cameron PA, 1999, MACROMOL RAPID COMM, V20, P616, DOI 10.1002/(SICI)1521-3927(19991201)20:12<616::AID-MARC616>3.0.CO