Model compounds based on poly(p-phenylenevinyleneborane) and terthiophene: Investigating the p–n junction in diblock copolymers

[1]  E. Kramer,et al.  A modular strategy for fully conjugated donor-acceptor block copolymers. , 2012, Journal of the American Chemical Society.

[2]  S. Darling,et al.  Supramolecular Conjugated Block Copolymers , 2012 .

[3]  F. Pammer,et al.  3-Vinylborane-functionalized oligothiophenes: isomer-dependent electronic structure and fluorescence enhancement upon anion binding , 2012 .

[4]  W. Huck,et al.  Synthesis, Purification, and Characterization of Well-Defined All-Conjugated Diblock Copolymers PF8TBT-b-P3HT , 2012 .

[5]  Robert J. Ono,et al.  Synthesis of conjugated diblock copolymers: two mechanistically distinct, sequential living polymerizations using a single catalyst , 2012 .

[6]  N. Greenham,et al.  Ternary photovoltaic blends incorporating an all-conjugated donor-acceptor diblock copolymer. , 2011, Nano letters.

[7]  Q. Qiao,et al.  Linker effects on optoelectronic properties of alternate donor–acceptor conjugated polymers , 2011 .

[8]  F. Jäkle,et al.  Synthesis and Characterization of Luminescent Polystyrene Derivatives with Sterically Protected Fluorenyl- and Carbazolylborane Moieties , 2011 .

[9]  Benjamin J. Leever,et al.  Synthesis and Characterization of Fully Conjugated Donor–Acceptor–Donor Triblock Copolymers , 2011 .

[10]  R. Lalancette,et al.  Applying the oligomer approach to luminescent conjugated organoboranes. , 2011, Journal of the American Chemical Society.

[11]  S. Darling,et al.  Optoelectronic Properties and Charge Transfer in Donor–Acceptor All-Conjugated Diblock Copolymers , 2011 .

[12]  F. Jäkle,et al.  Conjugated alternating copolymers with 4,4′-dimesitylboryl-2,2′-bithiophene as a building block , 2011 .

[13]  Robert J. Ono,et al.  Polythiophene–block–poly(γ-benzyl L-glutamate): synthesis and study of a new rod–rod block copolymer , 2011 .

[14]  K. Venkatasubbaiah,et al.  Synthesis and Electronic Structure of Ferrocenylborane-Modified Quaterthiophenes and Polythiophenes , 2011 .

[15]  S. Darling,et al.  Polythiophene-block-polyfluorene and Polythiophene-block-poly(fluorene-co-benzothiadiazole): Insights into the Self-Assembly of All-Conjugated Block Copolymers , 2011 .

[16]  S. Fabiano,et al.  Organoboron polymers for photovoltaic bulk heterojunctions. , 2010, Macromolecular rapid communications.

[17]  F. Jäkle.  Advances in the synthesis of organoborane polymers for optical, electronic, and sensory applications. , 2010, Chemical reviews.

[18]  S. Darling,et al.  Minimizing lateral domain collapse in etched poly(3-hexylthiophene)-block-polylactide thin films for improved optoelectronic performance. , 2010, Langmuir : the ACS journal of surfaces and colloids.

[19]  F. Jäkle,et al.  Donor-π-Acceptor Polymer with Alternating Triarylborane and Triphenylamine Moieties. , 2010, Macromolecular rapid communications.

[20]  Seth B. Darling,et al.  Optoelectronics using block copolymers , 2010 .

[21]  Xiao Feng,et al.  Receptor- and Ligand-Based Study on Novel 2, 2′-Bithienyl Derivatives as Non-Peptidic AANAT Inhibitors , 2010, J. Chem. Inf. Model..

[22]  Biwu Ma,et al.  Solution-Processable Crystalline Platinum-Acetylide Oligomers with Broadband Absorption for Photovoltaic Cells , 2010 .

[23]  Fosong Wang,et al.  Synthesis and characterization of phenylene-thiophene all-conjugated diblock copolymers , 2009 .

[24]  S. Darling.  Block copolymers for photovoltaics , 2009 .

[25]  R. Segalman,et al.  Block Copolymers for Organic Optoelectronics , 2009 .

[26]  Gaojian Chen,et al.  Macromolecular cobalt carbonyl complexes encapsulated in a click-cross-linked micelle structure as a nanoparticle to deliver cobalt pharmaceuticals. , 2009, Biomacromolecules.

[27]  Y. Chujo,et al.  Synthesis and Photostability of Poly(p-phenylenevinylene-borane)s , 2009 .

[28]  S. Darling,et al.  Self-Assembly of Poly(3-hexylthiophene)-block-polylactide Block Copolymer and Subsequent Incorporation of Electron Acceptor Material , 2009 .

[29]  J. Kobayashi,et al.  Enhancement of the Lewis acidity by substitution of sulfur-containing hetero aromatics in triarylboranes , 2009 .

[30]  F. Jäkle,et al.  Synthesis, Characterization, and Anion Binding of Redox-Active Triarylborane Polymers , 2009 .

[31]  R. Mezzenga,et al.  Crystalline Diblock Conjugated Copolymers: Synthesis, Self-Assembly, and Microphase Separation of Poly(3-butylthiophene)-b-poly(3-octylthiophene) , 2009 .

[32]  T. Emrick,et al.  Donor−Acceptor Poly(thiophene-block-perylene diimide) Copolymers: Synthesis and Solar Cell Fabrication , 2009 .

[33]  M. Lautens,et al.  A palladium-catalyzed approach to polycyclic sulfur heterocycles. , 2008, The Journal of organic chemistry.

[34]  M. Thelakkat,et al.  Crystalline-crystalline donor-acceptor block copolymers. , 2008, Angewandte Chemie.

[35]  Yongye Liang,et al.  Conjugated block copolymers and co-oligomers: from supramolecular assembly to molecular electronics , 2007 .

[36]  O. Fedorova,et al.  Synthesis, structures, and optical and electrochemical characteristics of novel crown-containing polythiophene systems , 2007 .

[37]  K. Venkatasubbaiah,et al.  Organoborane acceptor-substituted polythiophene via side-group borylation. , 2007, Journal of the American Chemical Society.

[38]  Cheng Zhang,et al.  Photovoltaic enhancement of organic solar cells by a bridged donor-acceptor block copolymer approach , 2007 .

[39]  H. Ohmiya,et al.  Cobalt-mediated cross-coupling reactions of primary and secondary alkyl halides with 1-(trimethylsilyl)ethenyl- and 2-trimethylsilylethynylmagnesium reagents. , 2006, Organic letters.

[40]  Rui Li,et al.  Design, Synthesis, and Characterization of a −Donor−Bridge−Acceptor−Bridge- Type Block Copolymer via Alkoxy- and Sulfone- Derivatized Poly(phenylenevinylenes) , 2006 .

[41]  R. D. Mccullough,et al.  Facile Synthesis of End-Functionalized Regioregular Poly(3-alkylthiophene)s via Modified Grignard Metathesis Reaction , 2005 .

[42]  P. Pale,et al.  Regio‐ and Chemoselective Coupling of Polyalkynes: A Convenient Access to Polyarylacetylenes and Polyenynes , 2005 .

[43]  Jun-ichi Hanna,et al.  High Carrier Mobility up to 0.1 cm2 V–1 s–1 at Ambient Temperatures in Thiophene‐Based Smectic Liquid Crystals , 2005 .

[44]  M. Melucci,et al.  Solution-phase microwave-assisted synthesis of unsubstituted and modified alpha-quinque- and sexithiophenes. , 2004, The Journal of organic chemistry.

[45]  Luping Yu,et al.  Synthesis of amphiphilic conjugated diblock oligomers as molecular diodes. , 2002, Angewandte Chemie.

[46]  B. Lin,et al.  Synthesis and characterization of conjugated diblock copolymers. , 2002, Chemistry.

[47]  Tomasz Kowalewski,et al.  Tuning the electrical conductivity and self-assembly of regioregular polythiophene by block copolymerization: nanowire morphologies in new di- and triblock copolymers. , 2002, Angewandte Chemie.

[48]  R. Cingolani,et al.  Oligothiophene isothiocyanates as a new class of fluorescent markers for biopolymers. , 2001, Journal of the American Chemical Society.

[49]  W. Paa,et al.  Intersystem crossing in oligothiophenes studied by fs time-resolved spectroscopy , 2000 .

[50]  K. Tamao,et al.  Tri-9-anthrylborane and Its Derivatives: New Boron-Containing π-Electron Systems with Divergently Extended π-Conjugation through Boron , 2000 .

[51]  Katz,et al.  From homoleptic to heteroleptic double stranded Copper(I) helicates: the role of self-recognition in self-assembly processes , 2000, The Journal of organic chemistry.

[52]  N. Matsumi,et al.  Synthesis of organoboron π-conjugated polymers by hydroboration polymerization between heteroaromatic diynes and mesitylborane and their light emitting properties , 1999 .

[53]  N. Matsumi,et al.  Synthesis of Poly(cyclodiborazane)s by Hydroboration Polymerization Using Mesitylborane , 1998 .

[54]  N. Matsumi,et al.  Extension of π-Conjugation Length via the Vacant p-Orbital of the Boron Atom. Synthesis of Novel Electron Deficient π-Conjugated Systems by Hydroboration Polymerization and Their Blue Light Emission , 1998 .

[55]  M. El-abadelah,et al.  SYNTHESIS OF THIOPHENE OLIGOMERS VIA ORGANOTIN COMPOUNDS , 1997 .

[56]  J. Tour,et al.  Convergent Synthetic Routes to Orthogonally Fused Conjugated Oligomers Directed toward Molecular Scale Electronic Device Applications. , 1996, The Journal of organic chemistry.

[57]  S. Jenekhe,et al.  Block Conjugated Copolymers: Toward Quantum-Well Nanostructures for Exploring Spatial Confinement Effects on Electronic, Optoelectronic, and Optical Phenomena , 1996 .

[58]  Zhao Jin,et al.  Hindered organoboron groups in organic synthesis. 17 [1]. Synthesis of 2,4,6‐triisopropylphenylborane (TripBH2)2, a useful alternative to thexylborane , 1992 .

[59]  T. E. Cole,et al.  Organoboranes. 49. An examination of convenient procedures for the generation of borane and monoalkyl- and dialkylboranes from lithium borohydride and monoalkyl- and dialkylborohydrides , 1986 .

[60]  T. E. Cole,et al.  Addition compounds of alkali-metal hydrides. 25. Rapid reaction of boronic esters and acids with lithium aluminum hydride. A novel and quantitative synthesis of lithium monoorganylborohydrides , 1984 .

[61]  Jian-wei Zhao,et al.  Asymmetric electron transport through a conjugated–saturated hydrocarbon molecular wire , 2011 .

[62]  Dae Won Cho,et al.  Synthesis and Properties of Soluble and Stable Silyl End-capped Bis-thienylanthracene Oligomers , 2007 .

[63]  J. Arnason,et al.  Synthesis and characterization of alkyl-, halo- and hetero-substituted derivatives of the potent phototoxin α-terthienyl , 1988 .