Year |
Citation |
Score |
2021 |
Hamzehpoor E, Ruchlin C, Tao Y, Ramos-Sanchez JE, Titi HM, Cosa G, Perepichka DF. Room Temperature Phosphorescence vs Triplet-Triplet Annihilation in N-Substituted Acridone Solids. The Journal of Physical Chemistry Letters. 6431-6438. PMID 34236197 DOI: 10.1021/acs.jpclett.1c01552 |
0.306 |
|
2020 |
Liu C, Hamzehpoor E, Sakai-Otsuka Y, Jadhav T, Perepichka DF. 90% Quantum Yield Pure-Red Doublet Emission from Stable, Colorless, Iodinated Triphenylmethane Solid. Angewandte Chemie (International Ed. in English). PMID 32822514 DOI: 10.1002/Anie.202009867 |
0.32 |
|
2020 |
Galeotti G, De Marchi F, Hamzehpoor E, MacLean O, Rajeswara Rao M, Chen Y, Besteiro LV, Dettmann D, Ferrari L, Frezza F, Sheverdyaeva PM, Liu R, Kundu AK, Moras P, Ebrahimi M, ... ... Perepichka DF, et al. Synthesis of mesoscale ordered two-dimensional π-conjugated polymers with semiconducting properties. Nature Materials. PMID 32424372 DOI: 10.1038/S41563-020-0682-Z |
0.387 |
|
2020 |
Niazi MR, Hamzehpoor E, Ghamari P, Perepichka IF, Perepichka DF. Nitroaromatics as n-type organic semiconductors for field effect transistors. Chemical Communications (Cambridge, England). PMID 32393948 DOI: 10.1039/D0Cc01236J |
0.376 |
|
2020 |
Jadhav T, Fang Y, Liu C, Dadvand A, Hamzehpoor E, Patterson W, Jonderian A, Stein RS, Perepichka DF. Transformation between 2D and 3D Covalent Organic Frameworks via Reversible [2+2] Cycloaddition. Journal of the American Chemical Society. PMID 32311256 DOI: 10.1021/Jacs.0C01990 |
0.332 |
|
2020 |
Fang Y, Lindner BD, Destoop I, Tsuji T, Zhang Z, Khaliullin RZ, Perepichka DF, Tahara K, De Feyter S, Tobe Y. Stereospecific Epitaxial Growth of Bilayered Porous Molecular Networks. Journal of the American Chemical Society. PMID 32306725 DOI: 10.1021/Jacs.0C00108 |
0.33 |
|
2020 |
Ali MU, Miao J, Cai J, Perepichka DF, Yang H, Meng H. Boosting the Efficiency and Curtailing the Efficiency Roll-off in Green Perovskite Light-Emitting Diodes via Incorporating Ytterbium as Cathode Interface Layer. Acs Applied Materials & Interfaces. PMID 32227978 DOI: 10.1021/Acsami.0C00950 |
0.445 |
|
2020 |
Yee N, Dadvand A, Perepichka DF. Serendipitous formation of semiconducting semi-NINDIGO indigoid by degradation of diindolopyrrole. The Journal of Organic Chemistry. PMID 32154715 DOI: 10.1021/Acs.Joc.0C00054 |
0.321 |
|
2020 |
Cui D, Perepichka DF, MacLeod JM, Rosei F. Surface-confined single-layer covalent organic frameworks: design, synthesis and application. Chemical Society Reviews. PMID 32141466 DOI: 10.1039/C9Cs00456D |
0.343 |
|
2020 |
Yao C, Zhao J, Zhu Y, Liu B, Yan C, Perepichka DF, Meng H. A Trifluoromethyl Group Modified Non-fullerene Acceptor Towards Improved Power Conversion Efficiency Over 13% in Polymer Solar Cells. Acs Applied Materials & Interfaces. PMID 32070091 DOI: 10.1021/Acsami.9B20544 |
0.526 |
|
2020 |
Fu C, Mikšátko J, Assies L, Vrkoslav V, Orlandi S, Kalbáč M, Kovaříček P, Zeng X, Zhou B, Muccioli L, Perepichka DF, Orgiu E. Surface-Confined Macrocyclization Dynamic Covalent Chemistry. Acs Nano. PMID 32068388 DOI: 10.1021/Acsnano.9B07671 |
0.342 |
|
2020 |
Lakshmi V, Liu CH, Rajeswara Rao M, Chen Y, Fang Y, Dadvand A, Hamzehpoor E, Sakai-Otsuka Y, Stein RS, Perepichka DF. A Two-dimensional Poly(azatriangulene) Covalent Organic Framework with Semiconducting and Paramagnetic States. Journal of the American Chemical Society. PMID 31948234 DOI: 10.1021/Jacs.9B11528 |
0.77 |
|
2020 |
Yao C, Zhu Y, Gu K, Zhao J, Ning J, Perepichka DF, Loo Y, Meng H. Fluorination of a polymer donor through the trifluoromethyl group for high-performance polymer solar cells Journal of Materials Chemistry A. 8: 12149-12155. DOI: 10.1039/D0Ta00098A |
0.449 |
|
2020 |
Pineda RF, Zems Y, Troughton J, Niazi MR, Perepichka DF, Watson T, Robertson N. Star-shaped triarylamine-based hole-transport materials in perovskite solar cells Sustainable Energy and Fuels. 4: 779-787. DOI: 10.1039/C9Se00366E |
0.303 |
|
2019 |
Mulay SV, Dishi O, Fang Y, Niazi MR, Shimon LJW, Perepichka DF, Gidron O. A macrocyclic oligofuran: synthesis, solid state structure and electronic properties. Chemical Science. 10: 8527-8532. PMID 32055302 DOI: 10.1039/C9Sc03247A |
0.439 |
|
2019 |
Perepichka DF, Hamzehpoor E. Crystal Engineering of Room Temperature Phosphorescence in Organic Solids. Angewandte Chemie (International Ed. in English). PMID 31725174 DOI: 10.1002/Anie.201913393 |
0.331 |
|
2019 |
Cui D, Fang Y, MacLean O, Perepichka DF, Rosei F, Clair S. Covalent organic frameworks from a monomer with reduced symmetry: polymorphism and Sierpiński triangles. Chemical Communications (Cambridge, England). PMID 31657366 DOI: 10.1039/C9Cc05674B |
0.326 |
|
2019 |
Liu CH, Niazi R, Perepichka DF. Extraordinary Enhancement of π-Electron Donor/Acceptor Ability by DD/AA Complementary Hydrogen Bonding. Angewandte Chemie (International Ed. in English). PMID 31560447 DOI: 10.1002/Anie.201910288 |
0.437 |
|
2019 |
De Marchi F, Galeotti G, Simenas M, Gallagher MC, Hamzehpoor E, MacLean O, Rao RM, Chen Y, Dettmann D, Contini G, Tornau EE, Ebrahimi M, Perepichka DF, Rosei F. Temperature-induced molecular reorganization on Au(111) driven by oligomeric defects. Nanoscale. PMID 31535121 DOI: 10.1039/C9Nr06117G |
0.383 |
|
2019 |
Che Y, Zhang Y, Yang Y, Liu CH, Izquierdo R, Xiao SS, Perepichka DF. Understanding photovoltaic behavior of A-D-A molecular semiconductors through a permutation of end groups. The Journal of Organic Chemistry. PMID 31380639 DOI: 10.1021/Acs.Joc.9B01654 |
0.361 |
|
2019 |
Jadhav T, Fang Y, Patterson W, Liu C, Hamzehpoor E, Perepichka DF. 2D Poly(arylene vinylene) Covalent Organic Frameworks via Aldol Condensation of Trimethyltriazine. Angewandte Chemie (International Ed. in English). PMID 31359568 DOI: 10.1002/Anie.201906976 |
0.396 |
|
2019 |
Harbers R, Heepenstrick T, Perepichka DF, Sokolowski M. Pure and mixed ordered monolayers of tetracyano-2,6-naphthoquinodimethane and hexathiapentacene on the Ag(100) surface. Beilstein Journal of Nanotechnology. 10: 1188-1199. PMID 31293856 DOI: 10.3762/Bjnano.10.118 |
0.399 |
|
2019 |
Galeotti G, De Marchi F, Taerum T, Besteiro LV, El Garah M, Lipton-Duffin J, Ebrahimi M, Perepichka DF, Rosei F. Surface-mediated assembly, polymerization and degradation of thiophene-based monomers. Chemical Science. 10: 5167-5175. PMID 31183070 DOI: 10.1039/C8Sc05267K |
0.395 |
|
2019 |
Galeotti G, Di Giovannantonio M, Cupo A, Xing S, Lipton-Duffin J, Ebrahimi M, Vasseur G, Kierren B, Fagot-Revurat Y, Tristant D, Meunier V, Perepichka DF, Rosei F, Contini G. An unexpected organometallic intermediate in surface-confined Ullmann coupling. Nanoscale. PMID 30946426 DOI: 10.1039/C9Nr00672A |
0.353 |
|
2019 |
Cao J, Wei X, Che Y, Li A, He Y, He C, Zhu Y, Chen X, Li T, Murtaza I, Yan L, Perepichka DF, Meng H. Polysiloxane–poly(vinyl alcohol) composite dielectrics for high-efficiency low voltage organic thin film transistors Journal of Materials Chemistry C. 7: 4879-4886. DOI: 10.1039/C9Tc00717B |
0.489 |
|
2018 |
Fang Y, Cibian M, Hanan GS, Perepichka DF, De Feyter S, Cuccia LA, Ivasenko O. Alkyl chain length effects on double-deck assembly at a liquid/solid interface. Nanoscale. PMID 30052249 DOI: 10.1039/C8Nr04220A |
0.695 |
|
2018 |
Goronzy DP, Ebrahimi M, Rosei F, Arramel, Fang Y, De Feyter S, Tait SL, Wang C, Beton PH, Wee ATS, Weiss PS, Perepichka DF. Supramolecular Assemblies on Surfaces: Nanopatterning, Functionality, and Reactivity. Acs Nano. PMID 30010321 DOI: 10.1021/Acsnano.8B03513 |
0.366 |
|
2018 |
Fu C, Orgiu E, Perepichka DF. Face-on vs. edge-on: tuning the structure of tetrathiafulvalene monolayers with solvent Journal of Materials Chemistry C. 6: 3787-3791. DOI: 10.1039/C7Tc05757A |
0.315 |
|
2017 |
Macleod JM, Lipton-Duffin J, Fu C, Taerum T, Perepichka DF, Rosei F. A 2D Substitutional Solid Solution Through Hydrogen-Bonding of Molecular Building Blocks. Acs Nano. PMID 28806527 DOI: 10.1021/Acsnano.7B03172 |
0.392 |
|
2017 |
Galeotti G, Di Giovannantonio M, Lipton-Duffin J, Ebrahimi M, Tebi S, Verdini A, Floreano L, Fagot-Revurat Y, Perepichka DF, Rosei F, Contini G. The role of halogens in on-surface Ullmann polymerization. Faraday Discussions. PMID 28770938 DOI: 10.1039/C7Fd00099E |
0.372 |
|
2017 |
Kynaston EL, Fang Y, Manion JG, Obhi NK, Howe JY, Perepichka DF, Seferos DS. Patchy Nanofibers from the Thin Film Self-Assembly of a Conjugated Diblock Copolymer. Angewandte Chemie (International Ed. in English). PMID 28206692 DOI: 10.1002/Anie.201700134 |
0.335 |
|
2017 |
Rao MR, Fang Y, De Feyter S, Perepichka DF. Conjugated Covalent Organic Frameworks via Michael Addition‒Elimination. Journal of the American Chemical Society. PMID 28088854 DOI: 10.1021/Jacs.6B12005 |
0.43 |
|
2017 |
Fu C, Beldon PJ, Perepichka DF. H-Bonding Control of Supramolecular Ordering of Diketopyrrolopyrroles Chemistry of Materials. 29: 2979-2987. DOI: 10.1021/Acs.Chemmater.6B05327 |
0.365 |
|
2017 |
Yan L, Popescu F, Rao MR, Meng H, Perepichka DF. A Wide Band Gap Naphthalene Semiconductor for Thin-Film Transistors Advanced Electronic Materials. 3: 1600556. DOI: 10.1002/Aelm.201600556 |
0.498 |
|
2016 |
Di Giovannantonio M, Tomellini M, Lipton-Duffin J, Galeotti G, Ebrahimi M, Cossaro A, Verdini A, Kharche N, Meunier V, Vasseur G, Fagot-Revurat Y, Perepichka DF, Rosei F, Contini G. Mechanistic Picture and Kinetic Analysis of Surface-Confined Ullmann Polymerization. Journal of the American Chemical Society. PMID 27958750 DOI: 10.1021/Jacs.6B09728 |
0.352 |
|
2016 |
Black HT, Yee N, Zems Y, Perepichka DF. Complementary Hydrogen Bonding Modulates Electronic Properties and Controls Self-Assembly of Donor/Acceptor Semiconductors. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27739184 DOI: 10.1002/Chem.201602543 |
0.416 |
|
2016 |
Mezour MA, Choueiri RM, Lukoyanova O, Lennox RB, Perepichka DF. Hydrogen bonding vs. molecule-surface interactions in 2D self-assembly of [C60]fullerenecarboxylic acids. Nanoscale. 8: 16955-16962. PMID 27714083 DOI: 10.1039/C6Nr04115A |
0.367 |
|
2016 |
Yan C, Zhao H, Perepichka DF, Rosei F. Lanthanide Ion Doped Upconverting Nanoparticles: Synthesis, Structure and Properties. Small (Weinheim An Der Bergstrasse, Germany). PMID 27345736 DOI: 10.1002/Smll.201601565 |
0.341 |
|
2016 |
Vasseur G, Fagot-Revurat Y, Sicot M, Kierren B, Moreau L, Malterre D, Cardenas L, Galeotti G, Lipton-Duffin J, Rosei F, Di Giovannantonio M, Contini G, Le Fèvre P, Bertran F, Liang L, ... ... Perepichka DF, et al. Quasi one-dimensional band dispersion and surface metallization in long-range ordered polymeric wires. Nature Communications. 7: 10235. PMID 26725974 DOI: 10.1038/Ncomms10235 |
0.421 |
|
2016 |
Cui D, MacLeod JM, Ebrahimi M, Perepichka DF, Rosei F. Solution and air stable host/guest architectures from a single layer covalent organic framework. Chemical Communications (Cambridge, England). 51: 16510-3. PMID 26417872 DOI: 10.1039/C5Cc07059G |
0.334 |
|
2016 |
Yu H, Guo Y, Yao C, Perepichka DF, Meng H. A smart polymer with a high sensitivity to temperature and humidity based on polyacrylamide hydrogel doped with polyiodide Journal of Materials Chemistry C. 4: 11055-11058. DOI: 10.1039/C6Tc04200G |
0.464 |
|
2016 |
Schneider JA, Perepichka DF. A new approach to polycyclic azaarenes: Visible-light photolysis of vinyl azides in the synthesis of diazabenzopyrene and diazaperylene Journal of Materials Chemistry C. 4: 7269-7276. DOI: 10.1039/C6Tc02046A |
0.344 |
|
2016 |
Yan L, Zhao Y, Yu H, Hu Z, He Y, Li A, Goto O, Yan C, Chen T, Chen R, Loo YL, Perepichka DF, Meng H, Huang W. Influence of heteroatoms on the charge mobility of anthracene derivatives Journal of Materials Chemistry C. 4: 3517-3522. DOI: 10.1039/C6Tc01088A |
0.541 |
|
2016 |
Fu C, Bélanger-Gariépy F, Perepichka DF. Supramolecular ordering of difuryldiketopyrrolopyrrole: the effect of alkyl chains and inter-ring twisting Crystengcomm. 18: 4285-4289. DOI: 10.1039/C6Ce00383D |
0.335 |
|
2016 |
McKeown GR, Fang Y, Obhi NK, Manion JG, Perepichka DF, Seferos DS. Synthesis of Macrocyclic Poly(3-hexylthiophene) and Poly(3-heptylselenophene) by Alkyne Homocoupling Acs Macro Letters. 5: 1075-1079. DOI: 10.1021/Acsmacrolett.6B00603 |
0.34 |
|
2016 |
Mezour MA, Voznyy O, Sargent EH, Lennox RB, Perepichka DF. Controlling C60 Organization through Dipole-Induced Band Alignment at Self-Assembled Monolayer Interfaces Chemistry of Materials. 28: 8322-8329. DOI: 10.1021/Acs.Chemmater.6B03527 |
0.374 |
|
2016 |
Fu C, Lin HP, Macleod JM, Krayev A, Rosei F, Perepichka DF. Unravelling the Self-Assembly of Hydrogen Bonded NDI Semiconductors in 2D and 3D Chemistry of Materials. 28: 951-961. DOI: 10.1021/Acs.Chemmater.5B04706 |
0.37 |
|
2016 |
Liu R, Fu C, Perepichka DF, Gallagher MC. Supramolecular structures of halogenated oligothiophenes on the Si(111)-√×√3-Ag surface Surface Science. 647: 51-54. DOI: 10.1016/J.Susc.2015.12.001 |
0.327 |
|
2016 |
Guo Y, Li W, Yu H, Perepichka DF, Meng H. Flexible Asymmetric Supercapacitors via Spray Coating of a New Electrochromic Donor-Acceptor Polymer Advanced Energy Materials. 7: 1601623. DOI: 10.1002/Aenm.201601623 |
0.459 |
|
2015 |
Rao MR, Black HT, Perepichka DF. Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene. Organic Letters. 17: 4224-7. PMID 26284538 DOI: 10.1021/Acs.Orglett.5B02009 |
0.403 |
|
2015 |
Schneider JA, Black H, Lin HP, Perepichka DF. Polymorphism in new thienothiophene-thiazolothiazole organic semiconductors. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 16: 1173-8. PMID 25808058 DOI: 10.1002/Cphc.201500066 |
0.353 |
|
2015 |
Rao MR, Desmecht A, Perepichka DF. π-Extended indenofluorenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 6193-201. PMID 25753783 DOI: 10.1002/Chem.201406646 |
0.353 |
|
2015 |
Mezour MA, Perepichka II, Ivasenko O, Lennox RB, Perepichka DF. Tridentate benzylthiols on Au(111): control of self-assembly geometry. Nanoscale. 7: 5014-22. PMID 25695677 DOI: 10.1039/C4Nr07207C |
0.705 |
|
2015 |
Dinca LE, MacLeod JM, Lipton-Duffin J, Fu C, Ma D, Perepichka DF, Rosei F. Tailoring the Reaction Path in the On-Surface Chemistry of Thienoacenes The Journal of Physical Chemistry C. 119: 22432-22438. DOI: 10.1021/Acs.Jpcc.5B05418 |
0.302 |
|
2014 |
Higgins S, Hodgkiss J, Plank N, Torsi L, Cowper P, Malliaras G, Braeken Y, Laurand N, Samuel I, Pomorska A, Wudl F, Xu B, Lemmer U, Perepichka D, Mount A, et al. Organic bioelectronics: general discussion. Faraday Discussions. 174: 413-28. PMID 25408300 DOI: 10.1039/C4Fd90048K |
0.397 |
|
2014 |
Higgins S, Torsi L, Whitworth G, Laurand N, Zhang S, Samuel I, Ebenhoch B, Wudl F, Frey G, Bucinskas A, Inigo J, Perepichka D, Lemmer U, Skabara P, Ottosson H, et al. Photonics: general discussion. Faraday Discussions. 174: 235-53. PMID 25408243 DOI: 10.1039/C4Fd90047B |
0.38 |
|
2014 |
Hodgkiss J, Conboy G, Hutchings G, Higgins S, Galbraith I, Findlay N, Taylor R, Salle M, Zhang S, Frey G, Bâldea I, Samuel I, Ebenhoch B, Wudl F, Turak A, ... ... Perepichka D, et al. Organic photovoltaics and energy: general discussion. Faraday Discussions. 174: 341-55. PMID 25406589 DOI: 10.1039/C4Fd90050B |
0.421 |
|
2014 |
Hodgkiss J, Zysman-Colman E, Higgins S, Solomon G, Bâldea I, Samuel I, Venkataraman L, Wudl F, Xu B, Venkatramani R, Ottosson H, Perepichka D, Lemmer U, Skabara P, Mount A, et al. Molecular electronics: general discussion. Faraday Discussions. 174: 125-51. PMID 25406517 DOI: 10.1039/C4Fd90049A |
0.496 |
|
2014 |
Black HT, Lin H, Bélanger-Gariépy F, Perepichka DF. Supramolecular control of organic p/n-heterojunctions by complementary hydrogen bonding. Faraday Discussions. 174: 297-312. PMID 25263229 DOI: 10.1039/C4Fd00133H |
0.414 |
|
2014 |
Dinca LE, MacLeod JM, Lipton-Duffin J, Fu C, Ma D, Perepichka DF, Rosei F. Tip-induced C-H activation and oligomerization of thienoanthracenes. Chemical Communications (Cambridge, England). 50: 8791-3. PMID 24967741 DOI: 10.1039/C4Cc03719G |
0.324 |
|
2014 |
Shi ZF, Black HT, Dadvand A, Perepichka DF. Pentacenobis(thiadiazole)dione, an n-type semiconductor for field-effect transistors. The Journal of Organic Chemistry. 79: 5858-60. PMID 24870358 DOI: 10.1021/Jo500760C |
0.345 |
|
2014 |
Mezour MA, Perepichka II, Zhu J, Lennox RB, Perepichka DF. Directing the assembly of gold nanoparticles with two-dimensional molecular networks. Acs Nano. 8: 2214-22. PMID 24512203 DOI: 10.1021/Nn405357J |
0.31 |
|
2014 |
Black HT, Perepichka DF. Crystal engineering of dual channel p/n organic semiconductors by complementary hydrogen bonding. Angewandte Chemie (International Ed. in English). 53: 2138-42. PMID 24500891 DOI: 10.1002/Anie.201310902 |
0.423 |
|
2014 |
Gutzler R, Cardenas L, Lipton-Duffin J, El Garah M, Dinca LE, Szakacs CE, Fu C, Gallagher M, Vondrá?ek M, Rybachuk M, Perepichka DF, Rosei F. Ullmann-type coupling of brominated tetrathienoanthracene on copper and silver. Nanoscale. 6: 2660-8. PMID 24441565 DOI: 10.1039/C3Nr05710K |
0.334 |
|
2014 |
Shuai Q, Black HT, Dadvand A, Perepichka DF. Dithienonaphthothiadiazole semiconductors: Synthesis, properties, and application to ambipolar field effect transistors Journal of Materials Chemistry C. 2: 3972-3979. DOI: 10.1039/C4Tc00094C |
0.388 |
|
2014 |
Gatti R, MacLeod JM, Lipton-Duffin JA, Moiseev AG, Perepichka DF, Rosei F. Substrate, molecular structure, and solvent effects in 2D self-assembly via hydrogen and halogen bonding Journal of Physical Chemistry C. 118: 25505-25516. DOI: 10.1021/Jp507729W |
0.402 |
|
2014 |
Perepichka DF, Perepichka IF, Wudl F. Cover Picture: Special Issue on Organic Electronics: In Memory of Prof. Michael Bendikov (1971-2013) (Isr. J. Chem. 5-6/2014) Israel Journal of Chemistry. 54: 413-413. DOI: 10.1002/Ijch.201490009 |
0.454 |
|
2014 |
Perepichka DF, Perepichka IF, Wudl F. Special Issue on Organic Electronics: In Memory of Prof. Michael Bendikov (1971-2013) Israel Journal of Chemistry. 54: 426-428. DOI: 10.1002/Ijch.201410008 |
0.45 |
|
2014 |
Blayney AJ, Perepichka IF, Wudl F, Perepichka DF. Advances and challenges in the synthesis of poly(p-phenylene vinylene)-based polymers Israel Journal of Chemistry. 54: 674-688. DOI: 10.1002/Ijch.201400067 |
0.488 |
|
2013 |
Zems Y, Moiseev AG, Perepichka DF. Convenient synthesis of a highly soluble and stable phosphorescent platinum porphyrin dye. Organic Letters. 15: 5330-3. PMID 24099151 DOI: 10.1021/Ol402590C |
0.311 |
|
2013 |
Gutzler R, Perepichka DF. π-Electron conjugation in two dimensions. Journal of the American Chemical Society. 135: 16585-94. PMID 24047465 DOI: 10.1021/Ja408355P |
0.406 |
|
2013 |
Di Giovannantonio M, El Garah M, Lipton-Duffin J, Meunier V, Cardenas L, Fagot Revurat Y, Cossaro A, Verdini A, Perepichka DF, Rosei F, Contini G. Insight into organometallic intermediate and its evolution to covalent bonding in surface-confined ullmann polymerization. Acs Nano. 7: 8190-8. PMID 23987501 DOI: 10.1021/Nn4035684 |
0.375 |
|
2013 |
MacLeod JM, Ben Chaouch Z, Perepichka DF, Rosei F. Two-dimensional self-assembly of a symmetry-reduced tricarboxylic acid. Langmuir : the Acs Journal of Surfaces and Colloids. 29: 7318-24. PMID 23327627 DOI: 10.1021/La3047593 |
0.385 |
|
2013 |
Dinca LE, Fu C, Macleod JM, Lipton-Duffin J, Brusso JL, Szakacs CE, Ma D, Perepichka DF, Rosei F. Unprecedented transformation of tetrathienoanthracene into pentacene on Ni(111). Acs Nano. 7: 1652-7. PMID 23327546 DOI: 10.1021/Nn305572S |
0.313 |
|
2013 |
Dadvand A, Sun W, Moiseev AG, Bélanger-Gariépy F, Rosei F, Meng H, Perepichka DF. 1,5-, 2,6- and 9,10-distyrylanthracenes as luminescent organic semiconductors Journal of Materials Chemistry C. 1: 2817. DOI: 10.1039/C3Tc30247D |
0.545 |
|
2013 |
Gidron O, Dadvand A, Wei-Hsin Sun E, Chung I, Shimon LJW, Bendikov M, Perepichka DF. Oligofuran-containing molecules for organic electronics Journal of Materials Chemistry C. 1: 4358-4367. DOI: 10.1039/C3Tc00079F |
0.66 |
|
2013 |
Cardenas L, Gutzler R, Lipton-Duffin J, Fu C, Brusso JL, Dinca LE, Vondrá?ek M, Fagot-Revurat Y, Malterre D, Rosei F, Perepichka DF. Synthesis and electronic structure of a two dimensional π-conjugated polythiophene Chemical Science. 4: 3263-3268. DOI: 10.1039/C3Sc50800E |
0.409 |
|
2013 |
Black HT, Dadvand A, Liu S, Ashby VS, Perepichka DF. Perfluoroalkyl-substitution versus electron-deficient building blocks in design of oligothiophene semiconductors Journal of Materials Chemistry C. 1: 260-267. DOI: 10.1039/C2Tc00032F |
0.381 |
|
2013 |
Schneider JA, Dadvand A, Wen W, Perepichka DF. Tuning the electronic properties of poly(thienothiophene vinylene)s via alkylsulfanyl and alkylsulfonyl substituents Macromolecules. 46: 9231-9239. DOI: 10.1021/Ma402018N |
0.382 |
|
2012 |
Gutzler R, Fu C, Dadvand A, Hua Y, MacLeod JM, Rosei F, Perepichka DF. Halogen bonds in 2D supramolecular self-assembly of organic semiconductors. Nanoscale. 4: 5965-71. PMID 22895808 DOI: 10.1039/C2Nr31648J |
0.384 |
|
2012 |
Fu C, Rosei F, Perepichka DF. 2D self-assembly of fused oligothiophenes: molecular control of morphology. Acs Nano. 6: 7973-80. PMID 22871038 DOI: 10.1021/Nn3025139 |
0.349 |
|
2012 |
Djukic B, Perepichka DF. Unexpected formation of a cyclic vinylene sulfate in the synthesis of ethynyl-substituted acenes. Chemical Communications (Cambridge, England). 48: 6651-3. PMID 22635168 DOI: 10.1039/C2Cc32805D |
0.352 |
|
2012 |
Dadvand A, Moiseev AG, Sawabe K, Sun WH, Djukic B, Chung I, Takenobu T, Rosei F, Perepichka DF. Maximizing field-effect mobility and solid-state luminescence in organic semiconductors. Angewandte Chemie (International Ed. in English). 51: 3837-41. PMID 22389133 DOI: 10.1002/Anie.201108184 |
0.327 |
|
2011 |
Djukic B, Perepichka DF. Non-classical heteroacenes: synthesis and properties of anthra[2,3-c:6,7-c']dithiophene derivatives. Chemical Communications (Cambridge, England). 47: 12619-21. PMID 22042513 DOI: 10.1039/C1Cc15623C |
0.361 |
|
2011 |
Gutzler R, Ivasenko O, Fu C, Brusso JL, Rosei F, Perepichka DF. Halogen bonds as stabilizing interactions in a chiral self-assembled molecular monolayer. Chemical Communications (Cambridge, England). 47: 9453-5. PMID 21776538 DOI: 10.1039/C1Cc13114A |
0.69 |
|
2011 |
Gidron O, Dadvand A, Sheynin Y, Bendikov M, Perepichka DF. Towards "green" electronic materials. α-Oligofurans as semiconductors. Chemical Communications (Cambridge, England). 47: 1976-8. PMID 21165466 DOI: 10.1039/C0Cc04699J |
0.647 |
|
2011 |
Ivasenko O, Perepichka DF. Mastering fundamentals of supramolecular design with carboxylic acids. Common lessons from X-ray crystallography and scanning tunneling microscopy. Chemical Society Reviews. 40: 191-206. PMID 20877909 DOI: 10.1039/C0Cs00022A |
0.699 |
|
2011 |
Eichhorn SH, Chen S, Ahmida M, Demenev A, Kayal H, Raad FS, Kaafarani BR, Patwardhan S, Grozema FC, Siebbeles LDA, Taerum T, Perepichka DF, Klenkler R. A combined study of mesomorphism, optical, and electronic properties of donor-acceptor columnar liquid crystals Proceedings of Spie - the International Society For Optical Engineering. 8114. DOI: 10.1117/12.893149 |
0.307 |
|
2011 |
Bendikov M, Martin N, Perepichka DF, Prato M. Fred Wudl. Discovering new science through making new molecules Journal of Materials Chemistry. 21: 1292-1294. DOI: 10.1039/C0Jm90123G |
0.574 |
|
2011 |
Kondratenko M, Moiseev AG, Perepichka DF. New stable donor–acceptor dyads for molecular electronics J. Mater. Chem.. 21: 1470-1478. DOI: 10.1039/C0Jm02545C |
0.391 |
|
2011 |
Lukoyanova O, Lepeltier M, Laferrière M, Perepichka DF. Donor-acceptor intermediates and low-bandgap polymers by electropolymerization of thienoazaborines Macromolecules. 44: 4729-4734. DOI: 10.1021/Ma200503F |
0.41 |
|
2010 |
Lepeltier M, Lukoyanova O, Jacobson A, Jeeva S, Perepichka DF. New azaborine-thiophene heteroacenes. Chemical Communications (Cambridge, England). 46: 7007-9. PMID 20730178 DOI: 10.1039/C0Cc01963A |
0.341 |
|
2010 |
Lipton-Duffin JA, Miwa JA, Kondratenko M, Cicoira F, Sumpter BG, Meunier V, Perepichka DF, Rosei F. Step-by-step growth of epitaxially aligned polythiophene by surface-confined reaction. Proceedings of the National Academy of Sciences of the United States of America. 107: 11200-4. PMID 20534511 DOI: 10.1073/Pnas.1000726107 |
0.402 |
|
2010 |
Demenev A, Eichhorn SH, Taerum T, Perepichka DF, Patwardhan S, Grozema FC, Siebbeles LDA, Klenkler R. Quasi temperature independent electron mobility in hexagonal columnar mesophases of an H-bonded benzotristhiophene derivative Chemistry of Materials. 22: 1420-1428. DOI: 10.1021/Cm902453Z |
0.379 |
|
2010 |
Perepichka DF, Bryce MR, Batsanov AS, Howard JAK, Cuello AO, Gray M, Rotello VM. ChemInform Abstract: Trialkyltetrathiafulvalene-σ-Tetracyanoanthraquinodimethane (R3TTF-σ-TCNAQ) Diads: Synthesis, Intramolecular Charge-Transfer Properties, and X-Ray Crystal Structure. Cheminform. 32: no-no. DOI: 10.1002/chin.200141150 |
0.427 |
|
2010 |
Mysyk DD, Perepichka IF, Perepichka DF, Bryce MR, Popov AF, Goldenberg LM, Moore AJ. ChemInform Abstract: Electron Acceptors of the Fluorene Series. Part 9. Derivatives of 9-(1,2-Dithiol-3-ylidene)-, 9-(1,3-Dithiol-2-ylidene)-, and 9-(1,3-Selenathiol-2-ylidene)fluorenes: Synthesis, Intramolecular Charge Transfer, and Redox Properties. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200001028 |
0.45 |
|
2010 |
PEREPICHKA IF, KUZ'MINA LG, PEREPICHKA DF, BRYCE MR, GOLDENBERG LM, POPOV AF, HOWARD JAK. ChemInform Abstract: Electron Acceptors of the Fluorene Series. Part 7. 2,7-Dicyano-4,5-dinitro-9-X-fluorenes: Synthesis, Cyclic Voltammetry, Charge Transfer Complexation with N-Propylcarbazole in Solution, and X-Ray Crystal Structures of Two Tetrathiaful Cheminform. 30: no-no. DOI: 10.1002/CHIN.199905103 |
0.44 |
|
2010 |
PEREPICHKA IF, PEREPICHKA DF, BRYCE MR, GOLDENBERG LM, KUZ'MINA LG, POPOV AF, CHESNEY A, MOORE AJ, HOWARD JAK, SOKOLOV NI. ChemInform Abstract: Fluorene Acceptors with Intramolecular Charge-Transfer from 1,3-Dithiole Donor Moieties: Novel Electron Transport Materials. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199832157 |
0.435 |
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2010 |
Jeeva S, Lukoyanova O, Karas A, Dadvand A, Rosei F, Perepichka DF. Highly emissive and electrochemically stable thienylene vinylene oligomers and copolymers: An unusual effect of alkylsulfanyl substituents (Advanced Functional Materials (2010) 20 (1661) DOI: 10.1002/adfm.201090057) Advanced Functional Materials. 20. DOI: 10.1002/Adfm.200902300 |
0.382 |
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2009 |
MacLeod JM, Ivasenko O, Fu C, Taerum T, Rosei F, Perepichka DF. Supramolecular ordering in oligothiophene-fullerene monolayers. Journal of the American Chemical Society. 131: 16844-50. PMID 19919147 DOI: 10.1021/Ja906206G |
0.705 |
|
2009 |
Taerum T, Lukoyanova O, Wylie RG, Perepichka DF. Synthesis, polymerization, and unusual properties of new star-shaped thiophene oligomers. Organic Letters. 11: 3230-3. PMID 19719178 DOI: 10.1021/Ol901127Q |
0.347 |
|
2009 |
Lipton-Duffin JA, Ivasenko O, Perepichka DF, Rosei F. Synthesis of polyphenylene molecular wires by surface-confined polymerization. Small (Weinheim An Der Bergstrasse, Germany). 5: 592-7. PMID 19241417 DOI: 10.1002/Smll.200801943 |
0.696 |
|
2009 |
Ivasenko O, Macleod JM, Chernichenko KY, Balenkova ES, Shpanchenko RV, Nenajdenko VG, Rosei F, Perepichka DF. Supramolecular assembly of heterocirculenes in 2D and 3D. Chemical Communications (Cambridge, England). 1192-4. PMID 19240870 DOI: 10.1039/B819532C |
0.684 |
|
2009 |
Perepichka DF, Rosei F. Chemistry. Extending polymer conjugation into the second dimension. Science (New York, N.Y.). 323: 216-7. PMID 19131618 DOI: 10.1126/Science.1165429 |
0.345 |
|
2009 |
Lepeltier M, Hiltz J, Lockwood T, Bélanger-Gariépy F, Perepichka DF. Towards crystal engineering of solid-state polymerization in dibromothiophenes Journal of Materials Chemistry. 19: 5167. DOI: 10.1039/B822997J |
0.356 |
|
2009 |
Lipton-Duffin JA, Ivasenko O, Perepichka DF, Rosei F. Surface polymerization: Small 5/2009 Small. 5: NA-NA. DOI: 10.1002/Smll.200990021 |
0.649 |
|
2008 |
Miwa JA, Cicoira F, Lipton-Duffin J, Perepichka DF, Santato C, Rosei F. Self-assembly of rubrene on Cu(111). Nanotechnology. 19: 424021. PMID 21832681 DOI: 10.1088/0957-4484/19/42/424021 |
0.325 |
|
2008 |
Clair S, Variola F, Kondratenko M, Jedrzejowski P, Nanci A, Rosei F, Perepichka DF. Self-assembled monolayer of alkanephosphoric acid on nanotextured Ti. The Journal of Chemical Physics. 128: 144705. PMID 18412469 DOI: 10.1063/1.2876421 |
0.317 |
|
2008 |
Perepichka DF, Perepichka IF, Ivasenko O, Moore AJ, Bryce MR, Kuz'mina LG, Batsanov AS, Sokolov NI. Combining high electron affinity and intramolecular charge transfer in 1,3-dithiole-nitrofluorene push-pull diads. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 2757-70. PMID 18240117 DOI: 10.1002/Chem.200701459 |
0.739 |
|
2008 |
Cicoira F, Santato C, Dadvand A, Harnagea C, Pignolet A, Bellutti P, Xiang Z, Rosei F, Meng H, Perepichka DF. Environmentally stable light emitting field effect transistors based on 2-(4-pentylstyryl)tetracene J. Mater. Chem.. 18: 158-161. DOI: 10.1039/B715324D |
0.422 |
|
2008 |
Miwa JA, Cicoira F, Bedwani S, Lipton-Duffin J, Perepichka DF, Rochefort A, Rosei F. Self-assembly of Rubrene on Copper Surfaces The Journal of Physical Chemistry C. 112: 10214-10221. DOI: 10.1021/Jp802762Q |
0.328 |
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2008 |
Brusso JL, Hirst OD, Dadvand A, Ganesan S, Cicoira F, Robertsons CM, Oakley RT, Rosei F, Perepichka DF. Two-dimensional structural motif in thienoacene semiconductors: Synthesis, structure, and properties of tetrathienoanthracene isomers Chemistry of Materials. 20: 2484-2494. DOI: 10.1021/Cm7030653 |
0.372 |
|
2007 |
Macleod JM, Ivasenko O, Perepichka DF, Rosei F. Stabilization of exotic minority phases in a multicomponent self-assembled molecular network. Nanotechnology. 18: 424031. PMID 21730463 DOI: 10.1088/0957-4484/18/42/424031 |
0.683 |
|
2007 |
Cicoira F, Miwa JA, Perepichka DF, Rosei F. Molecular assembly of rubrene on a metal/metal oxide nanotemplate. The Journal of Physical Chemistry. A. 111: 12674-8. PMID 17983212 DOI: 10.1021/Jp076090C |
0.336 |
|
2007 |
Perepichka DF, Rosei F. Metal nanoparticles: from "artificial atoms" to "artificial molecules". Angewandte Chemie (International Ed. in English). 46: 6006-8. PMID 17615605 DOI: 10.1002/Anie.200701554 |
0.302 |
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2007 |
Nath KG, Ivasenko O, MacLeod JM, Miwa JA, Wuest JD, Nanci A, Perepichka DF, Rosei F. Crystal engineering in two dimensions: An approach to molecular nanopatterning Journal of Physical Chemistry C. 111: 16996-17007. DOI: 10.1021/Jp0762774 |
0.672 |
|
2006 |
Nath KG, Ivasenko O, Miwa JA, Dang H, Wuest JD, Nanci A, Perepichka DF, Rosei F. Rational modulation of the periodicity in linear hydrogen-bonded assemblies of trimesic acid on surfaces Journal of the American Chemical Society. 128: 4212-4213. PMID 16568980 DOI: 10.1021/Ja0602896 |
0.67 |
|
2006 |
Wei Z, Kondratenko M, Dao LH, Perepichka DF. Rectifying diodes from asymmetrically functionalized single-wall carbon nanotubes. Journal of the American Chemical Society. 128: 3134-5. PMID 16522080 DOI: 10.1021/Ja053950Z |
0.302 |
|
2006 |
Amriou S, Wang C, Batsanov AS, Bryce MR, Perepichka DF, Ortí E, Viruela R, Vidal-Gancedo J, Rovira C. The interplay of inverted redox potentials and aromaticity in the oxidized states of new pi-electron donors: 9-(1,3-dithiol-2-ylidene)fluorene and 9-(1,3-dithiol-2-ylidene)thioxanthene derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 3389-400. PMID 16453366 DOI: 10.1002/Chem.200501326 |
0.516 |
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2005 |
Perepichka DF, Kondratenko M, Bryce MR. Self-assembly and multistage redox chemistry of strong electron acceptors on metal surfaces: polynitrofluorenes on gold and platinum. Langmuir : the Acs Journal of Surfaces and Colloids. 21: 8824-31. PMID 16142966 DOI: 10.1021/La051061J |
0.525 |
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2005 |
Zaman MB, Perepichka DF. A new simple synthesis of poly(thiophene-methine)s. Chemical Communications (Cambridge, England). 4187-9. PMID 16100598 DOI: 10.1039/B506138E |
0.342 |
|
2005 |
Perepichka DF, Bryce MR. Molecules with exceptionally small HOMO-LUMO gaps. Angewandte Chemie (International Ed. in English). 44: 5370-3. PMID 16034992 DOI: 10.1002/Anie.200500413 |
0.471 |
|
2005 |
Ho G, Heath JR, Kondratenko M, Perepichka DF, Arseneault K, Pézolet M, Bryce MR. The first studies of a tetrathiafulvalene-sigma-acceptor molecular rectifier. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 2914-22. PMID 15719357 DOI: 10.1002/Chem.200401121 |
0.501 |
|
2005 |
Ho G, Heath JR, Kondratenko M, Perepichka DF, Arseneault K, Pézolet M, Bryce MR. Cover Picture: The First Studies of a Tetrathiafulvalene-σ-Acceptor Molecular Rectifier (Chem. Eur. J. 10/2005) Chemistry - a European Journal. 11: 2883-2883. DOI: 10.1002/Chem.200590030 |
0.466 |
|
2005 |
Perepichka DF, Bryce MR. Moleküle mit sehr kleiner HOMO-LUMO-Energielücke Angewandte Chemie. 117: 5504-5507. DOI: 10.1002/Ange.200500413 |
0.477 |
|
2005 |
Perepichka IF, Perepichka DF, Meng H, Wudl F. Light-emitting polythiophenes Advanced Materials. 17: 2281-2305. DOI: 10.1002/Adma.200500461 |
0.579 |
|
2004 |
Bendikov M, Wudl F, Perepichka DF. Tetrathiafulvalenes, oligoacenenes, and their buckminsterfullerene derivatives: the brick and mortar of organic electronics. Chemical Reviews. 104: 4891-946. PMID 15535637 DOI: 10.1021/Cr030666M |
0.672 |
|
2004 |
Perepichka DF, Wudl F, Wilson SR, Sun Y, Schuster DI. The dissolution of carbon nanotubes in aniline, revisited Journal of Materials Chemistry. 14: 2749-2752. DOI: 10.1039/B403509G |
0.414 |
|
2003 |
Meng H, Perepichka DF, Bendikov M, Wudl F, Pan GZ, Yu W, Dong W, Brown S. Solid-state synthesis of a conducting polythiophene via an unprecedented heterocyclic coupling reaction. Journal of the American Chemical Society. 125: 15151-62. PMID 14653750 DOI: 10.1021/Ja037115Y |
0.731 |
|
2003 |
Perepichka DF, Bryce MR, Pearson C, Petty MC, McInnes EJ, Zhao JP. A covalent tetrathiafulvalene-tetracyanoquinodimethane diad: extremely low HOMO-LUMO gap, thermoexcited electron transfer, and high-quality langmuir-blodgett films. Angewandte Chemie (International Ed. in English). 42: 4636-9. PMID 14533150 DOI: 10.1002/Anie.200351876 |
0.471 |
|
2003 |
Perepichka DF, Bendikov M, Meng H, Wudl F. A one-step synthesis of a poly(iptycene) through an unusual Diels-Alder cyclization/dechlorination of tetrachloropentacene. Journal of the American Chemical Society. 125: 10190-1. PMID 12926939 DOI: 10.1021/Ja036193I |
0.724 |
|
2003 |
Meng H, Perepichka DF, Wudl F. Facile solid-state synthesis of highly conducting poly(ethylenedioxythiophene). Angewandte Chemie (International Ed. in English). 42: 658-61. PMID 12574998 DOI: 10.1002/Anie.200390181 |
0.575 |
|
2003 |
Bryce MR, Cooke G, Duclairoir FMA, John P, Perepichka DF, Polwart N, Rotello VM, Fraser Stoddart J, Tseng H. Surface confined pseudorotaxanes with electrochemically controllable complexation propertiesElectronic supplementary information (ESI) available: further experimental and theoretical data. See http://www.rsc.org/suppdata/jm/b3/b306274k/ Journal of Materials Chemistry. 13: 2111. DOI: 10.1039/B306274K |
0.515 |
|
2003 |
De Boer B, Meng H, Perepichka DF, Zheng J, Frank MM, Chabal YJ, Bao Z. Synthesis and characterization of conjugated mono- and dithiol oligomers and characterization of their self-assembled monolayers Langmuir. 19: 4272-4284. DOI: 10.1021/La0341052 |
0.54 |
|
2003 |
Meng H, Perepichka DF, Wudl F. Cover Picture: Facile Solid-State Synthesis of Highly Conducting Poly(ethylenedioxythiophene) (Angew. Chem. Int. Ed. 6/2003) Angewandte Chemie International Edition. 42: 589-589. DOI: 10.1002/Anie.200390169 |
0.577 |
|
2003 |
Meng H, Perepichka DF, Wudl F. Titelbild: Facile Solid-State Synthesis of Highly Conducting Poly(ethylenedioxythiophene) (Angew. Chem. 6/2003) Angewandte Chemie. 115: 609-609. DOI: 10.1002/Ange.200390137 |
0.577 |
|
2002 |
Perepichka DF, Bryce MR, Batsanov AS, McInnes EJ, Zhao JP, Farley RD. Engineering a remarkably low HOMO-LUMO gap by covalent linkage of a strong pi-donor and a pi-acceptor--tetrathiafulvalene-sigma-polynitrofluorene diads: their amphoteric redox behavior, electron transfer and spectroscopic properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4656-69. PMID 12561106 DOI: 10.1002/1521-3765(20021018)8:20<4656::Aid-Chem4656>3.0.Co;2-1 |
0.542 |
|
2002 |
Perepichka DF, Bryce MR, Perepichka IF, Lyubchik SB, Christensen CA, Godbert N, Batsanov AS, Levillain E, McInnes EJ, Zhao JP. A (pi-extended tetrathiafulvalene)-fluorene conjugate. Unusual electrochemistry and charge transfer properties: the first observation of a covalent D(2+)-sigma-A(.-) redox state(1). Journal of the American Chemical Society. 124: 14227-38. PMID 12440922 DOI: 10.1021/Ja012518O |
0.534 |
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2002 |
Brettreich M, Bendikov M, Chaffins S, Perepichka DF, Dautel O, Duong H, Helgeson R, Wudl F. Synthesis, X-ray structure, and properties of a tetrabenzannelated 1,2,4,5-cyclophane. Angewandte Chemie (International Ed. in English). 41: 3688-91; 3522. PMID 12370932 DOI: 10.1002/1521-3773(20021004)41:19<3688::Aid-Anie3688>3.0.Co;2-Q |
0.74 |
|
2002 |
Kuz’mina LG, Perepichka IF, Perepichka DF, Howard JAK, Bryce MR. Supramolecular architecture of two charge-transfer complexes based on 2,7-(X, X)-4,5-dinitro-9-dicyanomethylenefluorenes (X = NO2 or CN) and tetrathiafulvalene Crystallography Reports. 47: 251-261. DOI: 10.1134/1.1466501 |
0.432 |
|
2002 |
Batsanov AS, Perepichka DF. Methoxycarbonylmethyl 3-hydroxy-2-(methoxycarbonyl)benzo[b]furan-6-carboxylate Acta Crystallographica Section E Structure Reports Online. 58: o1227-o1228. DOI: 10.1107/S1600536802018524 |
0.314 |
|
2001 |
Batsanov AS, Collings JC, Howard JA, Marder TB, Perepichka DF. Arene-perfluoroarene interactions in crystal engineering. 5. Octafluoronaphthalene-tetrathiafulvalene (1/1). Acta Crystallographica. Section C, Crystal Structure Communications. 57: 1306-7. PMID 11706258 DOI: 10.1107/S0108270101013075 |
0.323 |
|
2001 |
Perepichka DF, Bryce MR, Batsanov AS, Howard JA, Cuello AO, Gray M, Rotello VM. Trialkyltetrathiafulvalene-sigma-tetracyanoanthraquinodimethane [R(3)TTF-sigma-TCNAQ] diads: synthesis, intramolecular charge-transfer properties, and X-ray crystal structure. The Journal of Organic Chemistry. 66: 4517-24. PMID 11421770 DOI: 10.1021/Jo001576+ |
0.563 |
|
2001 |
Perepichka DF, Bryce MR, McInnes EJ, Zhao JP. The first tetrathiafulvalene- sigma-polynitrofluorene diads: low HOMO-LUMO gap, amphoteric redox behavior, and charge transfer properties. Organic Letters. 3: 1431-4. PMID 11388834 DOI: 10.1021/Ol015581R |
0.497 |
|
2001 |
Jones AE, Christensen CA, Perepichka DF, Batsanov AS, Beeby A, Low PJ, Bryce MR, Parker AW. Photochemistry of the pi-extended 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene system: generation and characterisation of the radical cation, dication, and derived products. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 973-8. PMID 11303877 DOI: 10.1002/1521-3765(20010302)7:5<973::Aid-Chem973>3.0.Co;2-# |
0.484 |
|
2001 |
Perepichka IF, Perepichka DF, Lyubchik SB, Bryce MR, Batsanov AS, Howard JAK. Electron acceptors of the fluorene series. Part 13. 9-(5-Nitrofuran-2-ylidene)- and 9-(5-nitro-2-thienylidene)-2,4,5,7-tetranitrofluorenes: novel π-extended electron acceptors. Synthesis, cyclic voltammetry and X-ray crystal structures for the acceptor and its 4,5-dimethyltetrathiafulvalene complex, and a theoretical study Journal of the Chemical Society-Perkin Transactions 1. 1546-1551. DOI: 10.1039/B103392C |
0.554 |
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2001 |
Perepichka DF, Perepichka IF, Bryce MR, Sokolov NI, Moore AJ. π-Extended nitrofluorene-1,3-dithiole chromophore: enhancing the photoresponse of holographic materials through the balance of intramolecular charge transfer and electron affinity Journal of Materials Chemistry. 11: 1772-1774. DOI: 10.1039/B102081L |
0.522 |
|
2001 |
Perepichka D, Perepichka I, Bryce M, Moore A, Sokolov N. Pushûpull dithiole û fluorene acceptors as electron transport materials for holography Synthetic Metals. 121: 1487-1488. DOI: 10.1016/S0379-6779(00)01017-1 |
0.51 |
|
2001 |
Perepichka DF, Perepichka IF, Popov AF, Bryce MR, Batsanov AS, Chesney A, Howard JAK, Sokolov NI. Electron acceptors of the fluorene series Journal of Organometallic Chemistry. 637: 445-462. DOI: 10.1016/S0022-328X(01)00948-2 |
0.525 |
|
2001 |
Moore A, Chesney A, Bryce M, Batsanov A, Kelly J, Howard J, Perepichka I, Perepichka D, Meshulam G, Berkovic G, Kotler Z, Mazor R, Khodorkovsky V. Synthesis, Structures and Nonlinear Optical Properties of Novel D−π−A Chromophores: Intramolecular Charge Transfer from 1,3-Dithiole or Ferrocene Moieties to Polynitrofluorene or Dicyanomethylene Moieties through Conjugated Linkers European Journal of Organic Chemistry. 2001: 2671-2687. DOI: 10.1002/1099-0690(200107)2001:14<2671::Aid-Ejoc2671>3.0.Co;2-3 |
0.551 |
|
2001 |
Bryce M, Green A, Moore A, Perepichka D, Batsanov A, Howard J, Ledoux-Rak I, González M, Martín N, Segura J, Garín J, Orduna J, Alcalá R, Villacampa B. Synthesis of Conjugated Tetrathiafulvalene (TTF)-π-Acceptor Molecules − Intramolecular Charge Transfer and Nonlinear Optical Properties European Journal of Organic Chemistry. 2001: 1927-1935. DOI: 10.1002/1099-0690(200105)2001:10<1927::Aid-Ejoc1927>3.0.Co;2-4 |
0.547 |
|
1999 |
Mysyk DD, Perepichka IF, Perepichka DF, Bryce MR, Popov AF, Goldenberg LM, Moore AJ. Electron Acceptors of the Fluorene Series. 9.1Derivatives of 9-(1,2-Dithiol-3-ylidene)-, 9-(1,3-Dithiol-2-ylidene)-, and 9-(1,3-Selenathiol-2-ylidene)fluorenes: Synthesis, Intramolecular Charge Transfer, and Redox Properties The Journal of Organic Chemistry. 64: 6937-6950. DOI: 10.1021/Jo990100R |
0.527 |
|
1999 |
Perepichka I, Perepichka D, Bryce M, Chesney A, Popov A, Khodorkovsky V, Meshulam G, Kotler Z. Push-pull fluorene acceptors with ferrocene donor moiety Synthetic Metals. 102: 1558-1559. DOI: 10.1016/S0379-6779(98)00563-3 |
0.508 |
|
1998 |
Perepichka IF, Perepichka DF, Popov AF, Bryce MR, Goldenberg LM, Chesney A, Moore AJ, Howard JAK, Kuz’mina LG, Sokolov NI. Fluorene acceptors with intramolecular charge-transfer from 1,3-dithiole donor moieties: novel electron transport materials Chemical Communications. 819-820. DOI: 10.1039/A800912K |
0.511 |
|
1998 |
Perepichka IF, Kuz'mina LG, Perepichka DF, Bryce MR, Goldenberg LM, Popov AF, Howard JAK. Electron Acceptors of the Fluorene Series. 7.12,7-Dicyano-4,5-dinitro-9-X-fluorenes: Synthesis, Cyclic Voltammetry, Charge Transfer Complexation withN-Propylcarbazole in Solution, and X-ray Crystal Structures of Two Tetrathiafulvalene Complexes The Journal of Organic Chemistry. 63: 6484-6493. DOI: 10.1021/Jo9803481 |
0.535 |
|
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