Literature DB >> 14986943

Pyridine-containing m-phenylene ethynylene oligomers having tunable basicities.

Jennifer M Heemstra1, Jeffrey S Moore.   

Abstract

Incorporation of a pyridine monomer into the backbone of a m-phenylene ethynylene oligomer allows functionalization of the interior binding cavity of the folded oligomer. The basicity of the inwardly directed pyridine moiety was modulated by changing the substituents on the pyridine ring and through oligomer folding, granting access to a pK(a) range of 5-14 in acetonitrile. [reaction: see text]

Entities:  

Year:  2004        PMID: 14986943     DOI: 10.1021/ol0363016

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


  3 in total

1.  Anion-dependent fluorescence in bis(anilinoethynyl)pyridine derivatives: switchable ON-OFF and OFF-ON responses.

Authors:  Calden N Carroll; Brian A Coombs; Sean P McClintock; Charles A Johnson; Orion B Berryman; Darren W Johnson; Michael M Haley
Journal:  Chem Commun (Camb)       Date:  2011-04-07       Impact factor: 6.222

2.  Aryl C-H···Cl(-) hydrogen bonding in a fluorescent anion sensor.

Authors:  Blakely W Tresca; Lev N Zakharov; Calden N Carroll; Darren W Johnson; Michael M Haley
Journal:  Chem Commun (Camb)       Date:  2013-07-10       Impact factor: 6.222

3.  Substituent Effects on the [N-I-N](+) Halogen Bond.

Authors:  Anna-Carin C Carlsson; Krenare Mehmeti; Martin Uhrbom; Alavi Karim; Michele Bedin; Rakesh Puttreddy; Roland Kleinmaier; Alexei A Neverov; Bijan Nekoueishahraki; Jürgen Gräfenstein; Kari Rissanen; Máté Erdélyi
Journal:  J Am Chem Soc       Date:  2016-06-17       Impact factor: 15.419

  3 in total

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