Literature DB >> 12489955

Hydrogen bond-stabilized helix formation of a m-phenylene ethynylene oligomer.

Jennifer M Cary1, Jeffrey S Moore.   

Abstract

[reaction: see text] Incorporation of a single hydrogen bonded beta-turn mimic in the backbone of a m-phenylene ethynylene oligomer is shown to affect the thermodynamic properties of the folding reaction. Oligomers 1 and 2 both undergo solvophobic helix formation, but hydrogen bonded oligomer 1 was found to form a more stable helix with a higher tolerance to solvent denaturation than isomeric, non-hydrogen bonded oligomer 2.

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Year:  2002        PMID: 12489955     DOI: 10.1021/ol0270982

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


  3 in total

1.  Ion-mediated conformational switches.

Authors:  Peter C Knipe; Sam Thompson; Andrew D Hamilton
Journal:  Chem Sci       Date:  2014-11-21       Impact factor: 9.825

2.  H-Bonded Duplexes based on a Phenylacetylene Backbone.

Authors:  Jonathan A Swain; Giulia Iadevaia; Christopher A Hunter
Journal:  J Am Chem Soc       Date:  2018-09-04       Impact factor: 15.419

3.  Coordination-Directed Assembly of Luminescent Semiconducting Oligomers and Weak Interaction-Induced Morphology Transformation.

Authors:  Shiyin Zhao; Zhaoyang Ding; Chunfei Wang; Shichao Wang; Shun Li; Zuotai Zhang; Xuanjun Zhang
Journal:  ACS Omega       Date:  2019-08-20
  3 in total

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