Issue 11, 2015
From the journal:

Chemical Communications

Chemical design enables the control of conformational polymorphism in functional 2,3-thieno(bis)imide-ended materials†

Lucia Maini,*a   Federico Gallino,b   Massimo Zambianchi,c   Margherita Durso,c   Massimo Gazzano,c   Katia Rubini,a   Denis Gentili,d   Ilse Manet,c   Michele Muccini,de   Stefano Toffanin,d   Massimiliano Cavallinid  and  Manuela Melucci*c  

* Corresponding authors

a Dipartimento di Chimica “G. Ciamician”, Università di Bologna, Via F. Selmi 2, Bologna, Italy
E-mail: l.maini@unibo.it

b SAES-GETTERS S. p. A., Viale Italia 77, 20020 Lainate, MI, Italy

c Consiglio Nazionale delle Ricerche, Istituto per la Sintesi Organica e la Fotoreattività, (CNR-ISOF), via P. Gobetti 101, 40129 Bologna, Italy
E-mail: manuela.melucci@isof.cnr.it

d Consiglio Nazionale delle Ricerche, Istituto per lo Studio dei Materiali Nanostrutturati (CNR-ISMN), via P. Gobetti 101, 40129 Bologna, Italy

e E.T.C. s.r.l., via P. Gobetti 101, 40129 Bologna, Italy

Abstract

We report a successful chemical design strategy based on the even–odd alkyl end tailoring, which allows us to promote and control conformational polymorphism in single crystal and thin deposits of thienoimide-based molecular semiconductors (Cx-NT4N).

Graphical abstract: Chemical design enables the control of conformational polymorphism in functional 2,3-thieno(bis)imide-ended materials

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Article information

DOI
https://doi.org/10.1039/C4CC09177A
Article type
Communication
Submitted
17 Nov 2014
Accepted
19 Dec 2014
First published
19 Dec 2014

Chem. Commun., 2015,51, 2033-2035

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Chemical design enables the control of conformational polymorphism in functional 2,3-thieno(bis)imide-ended materials

L. Maini, F. Gallino, M. Zambianchi, M. Durso, M. Gazzano, K. Rubini, D. Gentili, I. Manet, M. Muccini, S. Toffanin, M. Cavallini and M. Melucci, Chem. Commun., 2015, 51, 2033 DOI: 10.1039/C4CC09177A

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