Bis-(salicylaldehyde-benzhydrylimino)nickel complexes with different electron groups: crystal structure and their catalytic properties toward (co)polymerization of norbornene and 1-hexene. Issue 63 (25th October 2018)

• Record Type: Journal Article
• Authors: He, Xiaohui; Tu, Guangshui; Zhang, Feng; Huang, Shengmei; Cheng, Changwen; Zhu, Chuanyi; Duan, Yapeng; Wang, Suli; Chen, Defu
• Is Part Of: RSC advances. Volume 8:Issue 63(2018)
• Page Start: 36298
• Page End: 36312
• Publication Date: 2018-10-25
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c8ra06561f
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Ni(ii ) complexes were successfully synthesized and characterized, and were highly active toward (co)polymerization of norbornene, and the 1-hexene content could be controlled. Abstract : Eight bis-(salicylaldehyde-benzhydrylimino)nickel complexes with different electron groups (Ni1–Ni8), Ni{(3-R1 )(5-R2 )C6 H2 (O)CHNCH(C6 H5 )2 }2, (R1 = H, R2 = H, Ni1; R1 = H, R2 = CH3, Ni2; R1 = H, R2 = OCH3, Ni3; R1 = H, R2 = Br, Ni4; R1 = CH3, R2 = H, Ni5; R1 = OCH3, R2 = H, Ni6; R1 = Br, R2 = Br, Ni7; R1 = Cl, R2 = Cl, Ni8), were synthesized and their crystal structures were characterized using single crystal X-ray diffraction. The results revealed that Ni1–Ni6 belong to the monoclinic system (space group P 2(1)/ n ), Ni7 belongs to the monoclinic system (space group C 2/ c ) and Ni8 belongs to the triclinic system (space group P 1̄). All nickel complexes exhibited high activities (0.46–2.07 × 10 6 gpolymer molNi −1 h −1 ) toward norbornene homopolymerization, and a strong electron-withdrawing group on the salicylaldimino aromatic ring can enhance the catalytic activity and favor polymerization. Ni1 and Ni2 exhibited high activities (0.55–2.40 × 10 5 gpolymer molNi −1 h −1 ) toward copolymerization of norbornene and 1-hexene in the presence of B(C6 F5 )3 . The 1-hexene content in the copolymers could be controlled up to 7.98–12.50% by varying the comonomer feed ratio of 1-hexene from 10 to 50%. It is observed that when the 5-position of the salicylaldimino aromatic ring has a substituent (–CH3 ), the 1-hexene insertion rate is lower than that without a substituent. In addition, the polymers showed high molecular weights (1.5–2.4 × 10 5 g mol −1 ) and narrow molecular weight distributions (1.62–1.89). The obtained polymers were also verified to be amorphous copolymers and had high thermal stability, good solubility and optical transparency.