Abstract
A series of aluminum alkyl complexes were synthesized and their catalytic polymerization reactivity toward 1-hexene was studied. Aluminum complexes, [C4H3N(CH2NHMe)-2]AlR2 (1a, R = Me; 1b, R = Et), containing substituted pyrrolyl ligand can be prepared by reacting AlR3 with one equiv of C4H3NH(CH 2NHMe)-2 in diethyl ether at room temperature. Dimeric aluminum complexes, {[C4H3N(CH2NMe)-2]AlR}2 (2a, R = Me; 2b, R = Et), can be obtained via metathesis by heating AlR 3 and with one equiv of [C4H3NH(CH 2NHMe)-2] in toluene for 24 h or via intramolecular methane elimination by heating 1 and 2 at 90 °C in toluene. Complexes 1a, 1b, 2a, and 2b have been characterized by NMR spectroscopy and by X-ray crystallography. Complexes 1a and 2a have shown moderate reactivity for 1-hexene polymerization in the presence of MAO.
Original language | English |
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Pages (from-to) | 1297-1302 |
Number of pages | 6 |
Journal | Journal of the Chinese Chemical Society |
Volume | 53 |
Issue number | 6 |
DOIs | |
Publication status | Published - 2006 Jan 1 |
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All Science Journal Classification (ASJC) codes
- Chemistry(all)
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Aluminum alkyl complexes containing bidentate, mono- or di-anionic pyrrolyl ligands : Intramolecular elimination of methane and 1-hexene polymerization. / Zhou, Chong Chin; Hung, Chen Hsiung; Huang, Jui-Hsien; Lee, Ting Yu.
In: Journal of the Chinese Chemical Society, Vol. 53, No. 6, 01.01.2006, p. 1297-1302.Research output: Contribution to journal › Article
TY - JOUR
T1 - Aluminum alkyl complexes containing bidentate, mono- or di-anionic pyrrolyl ligands
T2 - Intramolecular elimination of methane and 1-hexene polymerization
AU - Zhou, Chong Chin
AU - Hung, Chen Hsiung
AU - Huang, Jui-Hsien
AU - Lee, Ting Yu
PY - 2006/1/1
Y1 - 2006/1/1
N2 - A series of aluminum alkyl complexes were synthesized and their catalytic polymerization reactivity toward 1-hexene was studied. Aluminum complexes, [C4H3N(CH2NHMe)-2]AlR2 (1a, R = Me; 1b, R = Et), containing substituted pyrrolyl ligand can be prepared by reacting AlR3 with one equiv of C4H3NH(CH 2NHMe)-2 in diethyl ether at room temperature. Dimeric aluminum complexes, {[C4H3N(CH2NMe)-2]AlR}2 (2a, R = Me; 2b, R = Et), can be obtained via metathesis by heating AlR 3 and with one equiv of [C4H3NH(CH 2NHMe)-2] in toluene for 24 h or via intramolecular methane elimination by heating 1 and 2 at 90 °C in toluene. Complexes 1a, 1b, 2a, and 2b have been characterized by NMR spectroscopy and by X-ray crystallography. Complexes 1a and 2a have shown moderate reactivity for 1-hexene polymerization in the presence of MAO.
AB - A series of aluminum alkyl complexes were synthesized and their catalytic polymerization reactivity toward 1-hexene was studied. Aluminum complexes, [C4H3N(CH2NHMe)-2]AlR2 (1a, R = Me; 1b, R = Et), containing substituted pyrrolyl ligand can be prepared by reacting AlR3 with one equiv of C4H3NH(CH 2NHMe)-2 in diethyl ether at room temperature. Dimeric aluminum complexes, {[C4H3N(CH2NMe)-2]AlR}2 (2a, R = Me; 2b, R = Et), can be obtained via metathesis by heating AlR 3 and with one equiv of [C4H3NH(CH 2NHMe)-2] in toluene for 24 h or via intramolecular methane elimination by heating 1 and 2 at 90 °C in toluene. Complexes 1a, 1b, 2a, and 2b have been characterized by NMR spectroscopy and by X-ray crystallography. Complexes 1a and 2a have shown moderate reactivity for 1-hexene polymerization in the presence of MAO.
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U2 - 10.1002/jccs.200600173
DO - 10.1002/jccs.200600173
M3 - Article
AN - SCOPUS:34548569272
VL - 53
SP - 1297
EP - 1302
JO - Journal of the Chinese Chemical Society
JF - Journal of the Chinese Chemical Society
SN - 0009-4536
IS - 6
ER -