2014
DOI: 10.1039/c4tc00906a
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Nanostructured liquid-crystalline semiconductors – a new approach to soft matter electronics

Abstract: In contrast to solid-state organic semiconductors, superstructures can be constructed in liquidcrystalline (LC) phases, using chirality, hybridization with nanofibers, and nanosegregation. Chiral LC molecules form LC phases with helical structures. Gelator molecules self-assemble into fibrous aggregates in LC phases to form nanohybrid materials. Liquid crystal molecules consisting of π-conjugated moieties and incompatible functional parts form nanosegregated LC phases. These nanostructured π-conjugated LC mate… Show more

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Cited by 78 publications
(50 citation statements)
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“…[22][23][24][25][26] The design of novel π-conjugated polycyclic cores is therefore the key to improve the performances of liquid-crystalline (LC) semiconductors. In the last decade, LCs based on fused-thiophene subunits have been flourishing, and organic mesogenic derivatives of oligothiophenes, [27][28][29][30][31][32] thienothiophenes (TT), [33,34] dithienothiophenes (DTT), [35][36][37][38][39][40] benzothiophenes (BT), [41][42][43][44] benzotrithiophenes (BTT), [45,46] benzothieno [3,2-b]benzothiophene (BTBT), [47][48][49][50][51][52] materials have been amply reported. Such compounds exhibit high charge mobility with usual rates up to about 10 cm 2 V À 1 s À 1 for a rod-like mesogen [52] and nearly 0.2 cm 2 V À 1 s À 1 for a discotic mesogen, [45] in their highly ordered crystalline phases, directly obtained after annealing from their mesomorphic temperatures and slowly cooled down.…”
Section: Introductionmentioning
confidence: 99%
“…[22][23][24][25][26] The design of novel π-conjugated polycyclic cores is therefore the key to improve the performances of liquid-crystalline (LC) semiconductors. In the last decade, LCs based on fused-thiophene subunits have been flourishing, and organic mesogenic derivatives of oligothiophenes, [27][28][29][30][31][32] thienothiophenes (TT), [33,34] dithienothiophenes (DTT), [35][36][37][38][39][40] benzothiophenes (BT), [41][42][43][44] benzotrithiophenes (BTT), [45,46] benzothieno [3,2-b]benzothiophene (BTBT), [47][48][49][50][51][52] materials have been amply reported. Such compounds exhibit high charge mobility with usual rates up to about 10 cm 2 V À 1 s À 1 for a rod-like mesogen [52] and nearly 0.2 cm 2 V À 1 s À 1 for a discotic mesogen, [45] in their highly ordered crystalline phases, directly obtained after annealing from their mesomorphic temperatures and slowly cooled down.…”
Section: Introductionmentioning
confidence: 99%
“…Organic functional materials have attractive attentions because these materials are applied into inexpensive and flexible devices, compared to inorganic hard materials fabricated from silicone which is a representative substance for the development of 20th industry. [1][2][3][4][5] Among them, functional soft materials such as liquid crystals, [6][7][8][9][10] gels, [11][12][13][14][15][16] and polymers [5,[17][18][19][20] are candidates to develop organic electronics. For a construction of various self-organized superstructures in nano levels, molecular designs programmed by non-covalent intermolecular interactions such as hydrogen bondings, p-p interactions, van der Waals force, and nanosegregation are efficient strategies in condensed states.…”
mentioning
confidence: 99%
“…[15,16] In the LC phases, overlaps between π-molecular orbitals of the core parts produce charge transport. [30][31][32][33][34] M. Funahashi and T. Kato…”
Section: Mesogenic Units Based On Thiophene Ringsmentioning
confidence: 98%