daohang fenxiangbox searchbox qikanlogonew daohangnew searchboxnew navrightzone footerzone paper

Molecularly Imprinted Polymers for (Thio)urea Organocatalyst Recovery and Recycling AITranslate

Queen’s University Belfast; Queen’s University Belfast; Queen’s University Belfast; Queen’s University Belfast
AITranslate
Publisher: ACS
Share Citation Information Add to Favorites

    Scan to share on WeChat or Moments

Use WeChat scan.
Share with WeChat friends or Moments

Abstract AITranslate

The strong binding affinity of carboxylate-based ion pair monomers toward ureas and thioureas (>105 L mol–1 in DMSO-d6) has been utilized to prepare organocatalyst-selective molecularly imprinted polymers for the first time. These polymers exhibited exceptionally strong binding for the organocatalyst targets and were applied in the reversible capture of Schreiner’s urea and thiourea from reaction mixtures. Recycling and reuse of these precious homogeneous catalysts is achieved using rapid and straightforward solid-phase extraction protocols. Catalyst recoveries of up to 98% from Diels–Alder and Baylis–Hillman reactions are demonstrated, while the polymers themselves are stable for at least 100 extraction cycles without loss of performance.

KeyWords AITranslate

organocatalysis catalyst recycling molecular recognition molecular imprinting polymers solidphase extraction
No data

Basic Information:

DOI:https://doi.org/10.1021/acsapm.2c01308

Chinese Library Classification Number:

Citation Information:

The strong binding affinity of carboxylate-based ion pair monomers toward ureas and thioureas (>105 L mol–1 in DMSO-d6) has been utilized to prepare organocatalyst-selective molecularly imprinted polymers for the first time. These polymers exhibited exceptionally strong binding for the organocatalyst targets and were applied in the reversible capture of Schreiner’s urea and thiourea from reaction mixtures. Recycling and reuse of these precious homogeneous catalysts is achieved using rapid and straightforward solid-phase extraction protocols. Catalyst recoveries of up to 98% from Diels–Alder and Baylis–Hillman reactions are demonstrated, while the polymers themselves are stable for at least 100 extraction cycles without loss of performance.

quote

GB/T 7714-2015 [1] Federica Pessagno, Matthew Blair, Mark J. Muldoon, et al. ACS Applied Polymer Materials, 2022(4). DOI:10.1021/acsapm.2c01308.
MLA [1] Federica Pessagno, et al., ACS Applied Polymer Materials, no. 4, 2022, https://doi.org/10.1021/acsapm.2c01308.
APA [1] Federica Pessagno, Matthew Blair, Mark J. Muldoon, & Panagiotis Manesiotis. (2022). ACS Applied Polymer Materials(4). https://doi.org/10.1021/acsapm.2c01308
IEEE [1] Federica Pessagno, Matthew Blair, Mark J. Muldoon, and Panagiotis Manesiotis, ACS Applied Polymer Materials, no. 4, 2022, doi: 10.1021/acsapm.2c01308. keywords: {organocatalysis;catalyst recycling;molecular recognition;molecular imprinting;polymers;solidphase extraction}