2006
DOI: 10.1039/b517819c
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Conformational locking for band gap control in 3,4-propylenedioxythiophene based electrochromic polymers

Abstract: We report a tethered poly(3,4-propylenedioxythiophene) derivative with a built-in polymer conformation restriction which locks the conjugated chain at a specific dihedral angle, thus providing a handle in which to tune the optical and electronic properties of the material.

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Cited by 21 publications
(23 citation statements)
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“…[2][3][4] Furthermore, the polymers can be applied/processed/synthesized in a variety of different ways further increasing their utility. [5,6] By way of example, synthesis techniques such as in situ electro-polymerization, [7] vapor-phase polymerization (VPP), [8] or wet-chemical synthesis [9] are all commonly used.…”
Section: Introductionmentioning
confidence: 99%
“…[2][3][4] Furthermore, the polymers can be applied/processed/synthesized in a variety of different ways further increasing their utility. [5,6] By way of example, synthesis techniques such as in situ electro-polymerization, [7] vapor-phase polymerization (VPP), [8] or wet-chemical synthesis [9] are all commonly used.…”
Section: Introductionmentioning
confidence: 99%
“…Even though low-cost and low waste approaches to fabricate flexible ECDs are still yet to be obtained, these types of devices are considered to be the next generation of electronics. Moreover, bi-functional monomers with two thiophene active groups can impact properties such as color [ 15 ], conductivity, ion selectivity, and mechanical properties [ 16 , 17 , 18 ]. In this line, it has been reported the synthesis of the bis-malonyl EDOT that can be covalently attached to C 60 by cyclopropanation reaction and electrochemically deposited on an electrode, to produce novel ambipolar systems with new properties [ 19 , 20 ].…”
Section: Introductionmentioning
confidence: 99%
“…EDOT is a popular choice as a comonomer since it produces a low band gap polymer with high stability and good conductivity [22]. EDOT and its derivatives can give rise to non-covalent intramolecular interactions with adjacent thiophenic units and thus, induce self-rigidification of the conjugated system in which it is incorporated [23,24]. The resultant copolymer was characterized via cyclic voltammetry, FTIR and conductivity measurements.…”
Section: Introductionmentioning
confidence: 99%