Ring Opening Metathesis Polymerization (ROMP) of Norbornenes by (Arylimido)Niobium(V)–Alkylidene Catalysts, Nb(CHSiMe<sub>3</sub>)(NAr)[OC(CF<sub>3</sub>)<sub>3</sub>](PMe<sub>3</sub>)<sub>2</sub>
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- CHATCHAIPAIBOON Kanchana
- Dept. of Chemistry, Tokyo Metropolitan University
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- NOMURA Kotohiro
- Dept. of Chemistry, Tokyo Metropolitan University
Bibliographic Information
- Other Title
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- 芳香族イミドとフッ素化アルコキソ配位子を有するニオブ(V)–アルキリデン触媒によるノルボルネンおよびその誘導体の開環メタセシス重合
- Ring Opening Metathesis Polymerization (ROMP) of Norbornenes by (Arylimido)Niobium(Ⅴ)-Alkylidene Catalysts, Nb(CHSiMe₃)(NAr)[OC(CF₃)₃](PMe₃)₂
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Abstract
<p>Effects of arylimido ligands on the ring-opening metathesis polymerization (ROMP) of norbornene (NBE), norbornadiene (NBD), and tetracyclododecene (TCD) were investigated using a series of (arylimido)niobium(V)–alkylidene complex catalysts, Nb(CHSiMe3)(NAr)[OC(CF3)3](PMe3)2 [Ar = 2,6-Me2C6H3 (1), 2-MeC6H4 (2), 2,6-Cl2C6H3 (3)]. The catalytic activity in ROMP of NBE for 1 was higher than for 2 and 3 (toluene at 25 °C, initial NBE concentration 0.44 mmol/mL), and the activity increased at 50 °C. Further increase in the activity (TOF 236 s–1) was observed using 3 with addition of 1.0 equiv. of PMe3, and activity was higher than that for the analogous vanadium(V)–alkylidene. These complexes (1-3) could also catalyze ROMP of NBD and TCD and the activities were higher than that for the ROMP of NBE. The dichlorophenylimido analogue (3) showed the highest activity for the ROMP of TCD, whereas 1 showed higher activity than 2 and 3 for the ROMP of NBD.</p>
Journal
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- Journal of the Japan Petroleum Institute
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Journal of the Japan Petroleum Institute 64 (5), 238-244, 2021-09-01
The Japan Petroleum Institute
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Details 詳細情報について
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- CRID
- 1390289232191883520
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- NII Article ID
- 130008082549
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- NII Book ID
- AA11590615
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- ISSN
- 1349273X
- 13468804
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- NDL BIB ID
- 031702936
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed