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Journal articleMcCulloch I, Heeney M, Chabinyc ML, et al., 2009,
Semiconducting Thienothiophene Copolymers: Design, Synthesis, Morphology, and Performance in Thin-Film Organic Transistors
, ADVANCED MATERIALS, Vol: 21, Pages: 1091-1109, ISSN: 0935-9648- Author Web Link
- Open Access Link
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- Citations: 376
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Journal articleHamilton R, Smith J, Ogier S, et al., 2009,
High-Performance Polymer-Small Molecule Blend Organic Transistors
, ADVANCED MATERIALS, Vol: 21, Pages: 1166-1171, ISSN: 0935-9648- Author Web Link
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- Citations: 329
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Journal articleBrocorens P, Van Vooren A, Chabinyc ML, et al., 2009,
Solid-State Supramolecular Organization of Polythiophene Chains Containing Thienothiophene Units
, ADVANCED MATERIALS, Vol: 21, Pages: 1193-1198, ISSN: 0935-9648- Author Web Link
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- Citations: 71
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Journal articleBarard S, Heeney M, Chen L, et al., 2009,
Separate charge transport pathways determined by the time of flight method in bimodal polytriarylamine
, JOURNAL OF APPLIED PHYSICS, Vol: 105, ISSN: 0021-8979- Author Web Link
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- Citations: 29
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Journal articleShoaee S, An Z, Zhang X, et al., 2009,
Charge photogeneration in polythiophene-perylene diimide blend films
, CHEMICAL COMMUNICATIONS, Pages: 5445-5447, ISSN: 1359-7345- Author Web Link
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- Citations: 61
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Journal articleSmith J, Hamilton R, Heeney M, et al., 2008,
High-performance organic integrated circuits based on solution processable polymer-small molecule blends
, APPLIED PHYSICS LETTERS, Vol: 93, ISSN: 0003-6951- Author Web Link
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- Citations: 68
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Journal articleCrouch DJ, Skabara PJ, Heeney M, et al., 2008,
Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistors
, MACROMOLECULAR RAPID COMMUNICATIONS, Vol: 29, Pages: 1839-1843, ISSN: 1022-1336- Author Web Link
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- Citations: 22
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Journal articleMannsfeld SCB, Sharei A, Liu S, et al., 2008,
Highly Efficient Patterning of Organic Single-Crystal Transistors from the Solution Phase
, ADVANCED MATERIALS, Vol: 20, Pages: 4044-+, ISSN: 0935-9648- Author Web Link
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- Citations: 97
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Journal articleGrzegorczyk WJ, Savenije TJ, Heeney M, et al., 2008,
Relationship between Film Morphology, Optical, and Conductive Properties of Poly(thienothiophene): [6,6]-Phenyl C-61-Butyric Acid Methyl Ester Bulk Heterojunctions
, JOURNAL OF PHYSICAL CHEMISTRY C, Vol: 112, Pages: 15973-15979, ISSN: 1932-7447- Author Web Link
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- Citations: 18
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Journal articleNorthrup JE, Chabinyc ML, Hamilton R, et al., 2008,
Theoretical and experimental investigations of a polyalkylated-thieno[3,2-<i>b</i>]thiophene semiconductor
, JOURNAL OF APPLIED PHYSICS, Vol: 104, ISSN: 0021-8979- Author Web Link
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- Citations: 9
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Journal articleBallantyne AM, Chen L, Dane J, et al., 2008,
The effect of poly(3-hexylthiophene) molecular weight on charge transport and the performance of polymer:fullerene solar cells
, ADVANCED FUNCTIONAL MATERIALS, Vol: 18, Pages: 2373-2380, ISSN: 1616-301X- Author Web Link
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- Citations: 239
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Journal articleLi FM, Dhagat P, Haverinen HM, et al., 2008,
Polymer thin film transistor without surface pretreatment on silicon nitride gate dielectric
, APPLIED PHYSICS LETTERS, Vol: 93, ISSN: 0003-6951- Author Web Link
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- Citations: 6
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Journal articleDeLongchamp DM, Kline RJ, Jung Y, et al., 2008,
Molecular basis of mesophase ordering in a thiophene-based copolymer
, MACROMOLECULES, Vol: 41, Pages: 5709-5715, ISSN: 0024-9297- Author Web Link
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- Citations: 104
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PatentHeeney M, Zhang W, Tierney S, et al., 2008,
Polymers comprising fused selenophenes for use in optical, electrooptical and electronic devices
, WO 2008077465Disclosed is a polymer (I), wherein one of X1 and X2 is Se and the other one is S or Se, R1 and R2 are independently of each other identical or different groups selected from H, halogen, -CN, -NC, -NCO, - NCS, -OCN, -SCN, -C(=O)NR0R00, -C(=O)X0, -C(=O)R0, -NH2, -NR0R0, -SH, -SR0, -SO3H, -SO2R0, -OH, -NO2, -CF3, -SF5, P-Sp-, optionally substituted silyl, or carbyl or hydrocarbyl with 1 to 40 C atoms which is/are optionally substituted and optionally comprise one or more hetero atoms, P is a polymerizable group, Sp is a spacer group or a single bond, X0 is halogen, R0 and R00 are independently of each other H or an optionally substituted aliph. or arom. hydrocarbon group having 1 to 20 C atoms, Ar is in case of multiple occurrence independently of one another -CY1=CY2, acetylene or mono- or polynuclear aryl or heteroraryl which is optionally substituted, Y1 and Y2 are independently of each other H, F, Cl or CN, m is 0-4, and n is an integer > 10. The invention relates to polymers comprising fused selenophene rings, to their use as semiconductors or charge transport materials in optical, electrooptical or electronic devices, and to optical, electrooptical or electronic devices comprising them. In the examples of the invention, first 2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)selenopheno[3,2-b]thiophene was prepd. and (0.25 g, 0.56 mmol) of it was polymd. with (0.43 g, 0.56 mol) of 5,5'-dibromo-4,4'-dihexadecyl-2,2'-bithiophene by using Pd2[dba]3, tris-(tert-butyl) phosphine tetrafluoroborate and K2CO3 as catalysts, after pptn. and purifn. 0.37 g, 82 % of poly[5,5'-(4,4'-dihexadecyl-[2,2']bithiophene)-co-(selenopheno[3,2-b]thiophene)] was obtained.
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Journal articleLoo Y-L, McCulloch I, 2008,
Progress and challenges in commercialization of organic electronics
, MRS BULLETIN, Vol: 33, Pages: 653-662, ISSN: 0883-7694- Author Web Link
- Open Access Link
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- Citations: 95
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