Synthesis and characterization of dinuclear aluminum complexes bearing N,N-Dialkylaniline-amido ligands and its catalytic properties for lactone polymerization

Yancheng Han , Guangyun Zhu , Mengmeng Zhang , Shuai Wang , Wei Yao , Aihong Gao , Ping Lu

Chemical Research in Chinese Universities ›› 2014, Vol. 30 ›› Issue (5) : 874 -878.

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Chemical Research in Chinese Universities ›› 2014, Vol. 30 ›› Issue (5) : 874 -878. DOI: 10.1007/s40242-014-3507-2
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Synthesis and characterization of dinuclear aluminum complexes bearing N,N-Dialkylaniline-amido ligands and its catalytic properties for lactone polymerization

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Abstract

Two ligands [ortho-C6H4NR2(CH2NH)]2CH2CH2(3: R=Me; 4: R=Et) were prepared by the reduction of preligands [ortho-C6H4NR2(CH=N)]2CH2CH2(1: R=Me; 2: R=Et). These ligands reacted with AlMe3 to afford the corresponding dinuclear aluminum complexes {AlMe2[ortho-C6H4NR2(CH2N)]}2CH2CH2(5: R=Me; 6: R=Et). All the compounds were characterized by 1H and 13C nuclear magnetic resonance(NMR) spectroscopies and elemental analyses. The catalytic properties of the aluminum complexes towards the ring-opening polymerization of lactones were investigated in the presence of benzyl alcohol. All the polymerization reactions were proceeded in a controlled manner.

Keywords

Dinuclear aluminum / Ring-opening polymerization / Lactone

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Yancheng Han, Guangyun Zhu, Mengmeng Zhang, Shuai Wang, Wei Yao, Aihong Gao, Ping Lu. Synthesis and characterization of dinuclear aluminum complexes bearing N,N-Dialkylaniline-amido ligands and its catalytic properties for lactone polymerization. Chemical Research in Chinese Universities, 2014, 30(5): 874-878 DOI:10.1007/s40242-014-3507-2

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References

[1]

Drumright R E, Gruber P R, Henton D E. Adv. Mater., 2000, 12: 1841.

[2]

Mecking S. Angew. Chem. Int. Ed., 2004, 43: 1078.

[3]

Wei J C, Ma L L, Dai Y F, Chen Y W, Zhang P B, Cui Y, Chen X S. Chem. J. Chinese Universities, 2011, 32(11): 2674.

[4]

Platel R H, Hodgson L M, Williams C K. Polymer Reviews, 2008, 48: 11.

[5]

Stanford M J, Dove A P. Chem. Soc. Rev., 2010, 39: 486.

[6]

Thomas C M. Chem. Soc. Rev., 2010, 39: 165.

[7]

Wheaton C A, Hayes P G, Ireland B J. Dalton Trans., 2009, 4832.

[8]

Yao W, Cui N, Xue Y Z, Liu T T, Wang Y. Chem. Res. Chinese Universities, 2013, 29(1): 48.

[9]

Yao W, Xue Y Z, Liu T T, Gao A H, Wang Y F. Chem. Res. Chinese Universities, 2014, 30(1): 87.

[10]

Nomura N, Aoyama T, Ishii R, Kondo T. Macromolecules, 2005, 38: 5363.

[11]

Pappalardo D, Annunziata L, Pellecchia C. Macromolecules, 2009, 42: 6056.

[12]

Zhang W J, Wang Y H, Sun W H, Wang L, Redshaw C. Dalton Trans., 2012, 41: 11587.

[13]

Liu J, Iwasa N, Nomura K. Dalton Trans., 2008, 3978.

[14]

Yu X F, Wang Z X. Dalton Trans., 2013, 42: 3860.

[15]

Wang Y, Ma H Y. Chem. Commun., 2012, 48: 6729.

[16]

Chen H L, Dutta S, Huang P Y, Lin C C. Organometallics, 2012, 31: 2016.

[17]

Yao W, Mu Y, Gao A H, Gao W, Ye L. Dalton Trans., 2008, 3199.

[18]

Baran J, Duda A, Kowalski A, Szymanski R, Penczek S. Macromol. Rapid Commun., 1997, 18: 325.

[19]

Gao A H, Mu Y, Zhang J S, Yao W. Eur. J. Inorg. Chem., 2009, 3613.

[20]

Chamberlain B M, Cheng M, Moore D R, Ouitt T M, Lobovsky E B. J. Am. Chem. Soc., 2001, 123: 3229.

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