Literature DB >> 28731716

The Inheritance Angle: A Determinant for the Number of Members in the Substituted Cucurbit[n]uril Family.

Yi Zhao1, Vijaybabu Mandadapu1, Hasti Iranmanesh2, Jonathon E Beves2, Anthony I Day1.   

Abstract

Two new glycoluril diethers have been prepared, bearing strained cyclobutene and cyclobutane rings at the fused junction of the two imidazolidinone rings. The wide angle of the concave face of the cyclobutano derivative enabled the synthesis of cyclobutanocucurbit[5-8]uril, the largest member being the most significant achievement. A limited binding affinity study compared the new substituted family to classical cucurbit[5-8]uril. Surprisingly lower affinities were found, except for cyclobutanocucurbit[6]uril, which was 3.3-fold higher.

Entities:  

Year:  2017        PMID: 28731716     DOI: 10.1021/acs.orglett.7b01786

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Conformationally Mobile Acyclic Cucurbit[n]uril-Type Receptors Derived from an S-shaped Methylene Bridged Glycoluril Pentamer.

Authors:  Kimberly G Brady; Laura Gilberg; David Sigwalt; Joshua Bistany-Riebman; Steven Murkli; Jared Klemm; Petr Kulhánek; Vladimír Šindelář; Lyle Isaacs
Journal:  Supramol Chem       Date:  2020-08-13       Impact factor: 1.688

2.  Study on the coordination of cyclopentanocucurbit[5,6]uril with Fe3+, Co2+ and Ni2+ ions.

Authors:  Jun Zheng; Yue Ma; Xinan Yang; Peihua Ma
Journal:  RSC Adv       Date:  2022-06-28       Impact factor: 4.036

3.  The Cyclobutanocucurbit[5-8]uril Family: Electronegative Cavities in Contrast to Classical Cucurbituril while the Electropositive Outer Surface Acts as a Crystal Packing Driver.

Authors:  Minghua Chen; Naixia Lv; Weiwei Zhao; Anthony I Day
Journal:  Molecules       Date:  2021-12-03       Impact factor: 4.411

  3 in total

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