Abstract
The series of 2-(1-(2,4-dibenzhydrylnaphthylimino)ethyl)-6-(1-(arylimino)ethyl)pyridine derivatives and their cobalt chlorides (Co1−Co5) were synthesized and fully characterized. The representative complexes Co2 and Co3 were confirmed by single crystal X-ray diffraction analyses, indicating pseudo-square-pyramidal geometry around the cobalt centre. All cobalt complexes, activated with either methylaluminoxane (MAO) or modified methylaluminoxane (MMAO), exhibited high activities towards ethylene polymerization, and produced polyethylenes with high molecular weight and highly linear feature as well as unimodal distribution.
Similar content being viewed by others
References
Johnson LK, Killian CM, Brookhart M. J Am Chem Soc, 1995, 117: 6414–6415
Small BL, Brookhart M, Bennett AMA. J Am Chem Soc, 1998, 120: 4049–4050
Britovsek GJP, Gibson VC, McTavish SJ, Solan GA, White AJP, Williams DJ, Britovsek GJP, Kimberley BS, Maddox PJ. Chem Commun, 1998, 849–850
Bianchini C, Giambastiani G, Luconi L, Meli A. Coordin Chem Rev, 2010, 254: 431–455
Zhang W, Sun WH, Redshaw C. Dalton Trans, 2013, 42: 8988–8997
Ma J, Feng C, Wang S, Zhao KQ, Sun WH, Redshaw C, Solan GA. Inorg Chem Front, 2014, 1: 14–34
Flisak Z, Sun WH. ACS Catal, 2015, 5: 4713–4724
Guo L, Dai S, Sui X, Chen C. ACS Catal, 2016, 6: 428–441
Britovsek GJP, Bruce M, Gibson VC, Kimberley BS, Maddox PJ, Mastroianni S, McTavish SJ, Redshaw C, Solan GA, Strömberg S, White AJP, Williams DJ. J Am Chem Soc, 1999, 121: 8728–8740
Chen Y, Qian C, Sun J. Organomets, 2003, 22: 1231–1236
Sun WH, Jie S, Zhang S, Zhang W, Song Y, Ma H, Chen J, Wedeking K, Fröhlich R. Organomets, 2006, 25: 666–677
Jie S, Zhang S, Sun WH, Kuang X, Liu T, Guo J. J Mol Catal A-Chem, 2007, 269: 85–96
Zhang M, Hao P, Zuo W, Jie S, Sun WH. J Organomet Chem, 2008, 693: 483–491
Xiao L, Gao R, Zhang M, Li Y, Cao X, Sun WH. Organomets, 2009, 28: 2225–2233
Gao R, Wang K, Li Y, Wang F, Sun WH, Redshaw C, Bochmann M. J Mol Catal A-Chem, 2009, 309: 166–171
Gao R, Li Y, Wang F, Sun WH, Bochmann M. Eur J Inorg Chem, 2009, 2009: 4149–4156
Song S, Gao R, Zhang M, Li Y, Wang F, Sun WH. Inorg Chim Acta, 2011, 376: 373–380
Zhang W, Chai W, Sun WH, Hu X, Redshaw C, Hao X. Organomets, 2012, 31: 5039–5048
Sun WH, Kong S, Chai W, Shiono T, Redshaw C, Hu X, Guo C, Hao X. Appl Catal A-Gen, 2012, 447–448: 67–73
Appukuttan VK, Liu Y, Son BC, Ha CS, Suh H, Kim I. Organomets, 2011, 30: 2285–2294
Huang F, Xing Q, Liang T, Flisak Z, Ye B, Hu X, Yang W, Sun WH. Dalton Trans, 2014, 43: 16818–16829
Huang F, Zhang W, Yue E, Liang T, Hu X, Sun WH. Dalton Trans, 2016, 45: 657–666
Ba J, Du S, Yue E, Hu X, Flisak Z, Sun WH. RSC Adv, 2015, 5: 32720–32729
Barbaro P, Bianchini C, Giambastiani G, Rios IG, Meli A, Oberhauser W, Segarra AM, Sorace L, Toti A. Organomets, 2007, 26: 4639–4651
Sun WH, Xing Q, Yu J, Novikova E, Zhao W, Tang X, Liang T, Redshaw C. Organomets, 2013, 32: 2309–2318
Xing Q, Zhao T, Qiao Y, Wang L, Redshaw C, Sun WH. RSC Adv, 2013, 3: 26184–26193
Xing Q, Zhao T, Du S, Yang W, Liang T, Redshaw C, Sun WH. Organomets, 2014, 33: 1382–1388
Kaul FAR, Puchta GT, Frey GD, Herdtweck E, Herrmann WA. Organomets, 2007, 26: 988–999
Guo L, Gao H, Zhang L, Zhu F, Wu Q. Organomets, 2010, 29: 2118–2125
Yu J, Liu H, Zhang W, Hao X, Sun WH. Chem Commun, 2011, 47: 3257–3259
Yu J, Huang W, Wang L, Redshaw C, Sun WH. Dalton Trans, 2011, 40: 10209–10214
Zhao W, Yu J, Song S, Yang W, Liu H, Hao X, Redshaw C, Sun WH. Polymer, 2012, 53: 130–137
Lai J, Zhao W, Yang W, Redshaw C, Liang T, Liu Y, Sun WH. Polym Chem, 2012, 3: 787–793
Cao X, He F, Zhao W, Cai Z, Hao X, Shiono T, Redshaw C, Sun WH. Polymer, 2012, 53: 1870–1880
Wang S, Li B, Liang T, Redshaw C, Li Y, Sun WH. Dalton Trans, 2013, 42: 9188–9197
Liu H, Zhao W, Hao X, Redshaw C, Huang W, Sun WH. Organomets, 2011, 30: 2418–2424
Sun WH, Song S, Li B, Redshaw C, Hao X, Li YS, Wang F. Dalton Trans, 2012, 41: 11999–12010
Rhinehart JL, Brown LA, Long BK. J Am Chem Soc, 2013, 135: 16316–16319
Rhinehart JL, Mitchell NE, Long BK. ACS Catal, 2014, 4: 2501–2504
Dai S, Sui X, Chen C. Angew Chem Int Ed, 2015, 54: 9948–9953
Yue E, Zhang L, Xing Q, Cao XP, Hao X, Redshaw C, Sun WH. Dalton Trans, 2014, 43: 423–431
Yue E, Xing Q, Zhang L, Shi Q, Cao XP, Wang L, Redshaw C, Sun WH. Dalton Trans, 2014, 43: 3339–3346
Wen C, Yuan S, Shi Q, Yue E, Liu D, Sun WH. Organomets, 2014, 33: 7223–7231
Yue E, Zeng Y, Zhang W, Huang F, Cao XP, Liang T, Sun WH. Inorg Chim Acta, 2016, 442: 178–186
Sheldrick GM. SHELXTL–97. Program for the Refinement of Crystal Structures. Germany: University of Göttingen, 1997
Spek AL. Acta Crystlogr D, 2009, 65: 148–155
Xiao T, Hao P, Kehr G, Hao X, Erker G, Sun WH. Organomets, 2011, 30: 4847–4853
Ittel SD, Johnson LK, Brookhart M. Chem Rev, 2000, 100: 1169–1204
Tomov AK, Gibson VC, Britovsek GJP, Long RJ, van Meurs M, Jones DJ, Tellmann KP, Chirinos JJ. Organomets, 2009, 28: 7033–7040
Galland GB, Quijada R, Rojas R, Bazan G, Komon ZJA. Macromolecules, 2002, 35: 339–345
Author information
Authors and Affiliations
Corresponding author
Electronic supplementary material
11426_2016_157_MOESM1_ESM.docx
Highly linear polyethylenes using the 2-(1-(2,4-dibenzhydrylnaphthyl imino)ethyl)-6-(1-(arylimino)ethyl)pyridylcobalt chlorides: Synthesis, characterization and ethylene polymerization
Rights and permissions
About this article
Cite this article
Yue, E., Zeng, Y., Zhang, W. et al. Highly linear polyethylenes using the 2-(1-(2,4-dibenzhydrylnaphthylimino)ethyl)-6-(1-(arylimino)ethyl)-pyridylcobalt chlorides: synthesis, characterization and ethylene polymerization. Sci. China Chem. 59, 1291–1300 (2016). https://doi.org/10.1007/s11426-016-0157-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11426-016-0157-0