4.6 Article

Switching from linear to cyclic δ-Polyvalerolactone synthesized via zeolitic imidazolate framework as a catalyst: A promising approach

期刊

APPLIED ORGANOMETALLIC CHEMISTRY
卷 33, 期 5, 页码 -

出版社

WILEY
DOI: 10.1002/aoc.4890

关键词

biodegradable polymer; heterogeneous catalyst; Polyvalerolactone; ring opening polymerization; Zeolitic imidiazolate framework

资金

  1. Chinese Scholarship Council [2015GXZ386]
  2. Tomsk Polytechnic University Competitiveness Enhancement Program [VIU-2019]
  3. Russian Foundation for Basic Research [18-29-04047]
  4. State Key Lab of Advanced Technology for Materials Synthesis and Processing (Wuhan University of Technology)

向作者/读者索取更多资源

A series of spray dried zeolitic imidazolate frameworks (ZIFs = ZIF-8, ZIF-67, and Zn/Co-ZIF) are used as a catalyst for the bulk ring-opening polymerization of delta-valerolactone without any co-catalyst to generate polyvalerolactone. Interestingly, using the same catalyst under the same reaction conditions could manipulate the structure of the product polymer, and thus its physical properties. Thus, using a dried substrate leads to the formation of the cyclic polymer while a linear polymer was formed on using the commercially available substrate. An activated monomer mechanism has been suggested where the propagating zinc alkoxide undergoes an intramolecular transesterification to release cyclic or linear polyvalerolactone. The ROP of delta-VL without drying shows that the polymeric zwitterions have little tendency to cyclize in the presence of moisture. At 140 degrees C, ZIF-8 shows a superior catalytic activity resulting in the production of cyclic polyvalerolactone having a high molecular weight as compared to ZIF-67 or Zn/Co-ZIF due to the presence of highly active sites. The catalyst could be recycled and reused without any significant loss of catalytic activity.

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