Year |
Citation |
Score |
2020 |
Wałęsa-Chorab M, Skene WG. Engaging the Reversible Bonds of an Immobilized Styreno-Thiophene Film Crystal Growth & Design. 20: 5688-5697. DOI: 10.1021/Acs.Cgd.9B01235 |
0.337 |
|
2019 |
Hiscock LK, Yao C, Skene WG, Dawe LN, Maly KE. Synthesis of Emissive Heteroacene Derivatives via Nucleophilic Aromatic Substitution. The Journal of Organic Chemistry. PMID 31651162 DOI: 10.1021/Acs.Joc.9B02523 |
0.352 |
|
2019 |
Gautier Y, Maris T, Skene WG. Crystal structure of diethyl 2-amino-5-{4-[bis(4-methylphenyl)amino]benzamido}thiophene-3,4-dicarboxylate Acta Crystallographica Section E: Crystallographic Communications. 75: 589-592. PMID 31110792 DOI: 10.1107/S2056989019003864 |
0.343 |
|
2019 |
Bishop S, Tremblay MH, Gellé A, Skene WG. Understanding Color Tuning and Reversible Oxidation of Conjugated Azomethines. The Journal of Physical Chemistry. A. PMID 30892894 DOI: 10.1021/Acs.Jpca.8B10593 |
0.392 |
|
2019 |
Wałęsa-Chorab M, Skene WG. Investigation of an electroactive immobilized azomethine for potential electrochromic use Solar Energy Materials and Solar Cells. 200: 109977. DOI: 10.1016/J.Solmat.2019.109977 |
0.345 |
|
2019 |
Brodeur J, Hu L, Malinge A, Eizner E, Skene WG, Kéna‐Cohen S. Highly Efficient and Spectrally Narrow Near‐Infrared Fluorescent OLEDs Using a TADF‐Sensitized Cyanine Dye Advanced Optical Materials. 7: 1901144. DOI: 10.1002/Adom.201901144 |
0.346 |
|
2018 |
Hiscock LK, Raycraft B, Walesa-Chorab M, Cambe C, Malinge A, Skene WG, Taing H, Eichhorn SH, Dawe L, Maly K. Synthesis and Characterization of Liquid Crystalline Tetraoxapentacene Derivatives Exhibiting Aggregation-Induced Emission. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30335207 DOI: 10.1002/Chem.201804215 |
0.348 |
|
2017 |
Wałęsa-Chorab M, Skene WG. Visible-to-NIR Electrochromic Device Prepared from a Thermally Polymerizable Electroactive Organic Monomer Acs Applied Materials & Interfaces. 9: 21524-21531. PMID 28605193 DOI: 10.1021/Acsami.7B02903 |
0.396 |
|
2017 |
Tremblay M, Gellé A, Skene WG. Ambipolar azomethines as potential cathodic color switching materials New Journal of Chemistry. 41: 2287-2295. DOI: 10.1039/C6Nj01732K |
0.391 |
|
2016 |
Wałęsa-Chorab M, Tremblay MH, Skene WG. Hydrogen-Bond and Supramolecular-Contact Mediated Fluorescence Enhancement of Electrochromic Azomethines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27388588 DOI: 10.1002/Chem.201600859 |
0.429 |
|
2016 |
Tremblay MH, Skalski T, Gautier Y, Pianezzola G, Skene WG. Investigation of triphenylamine-thiophene-azomethine derivatives: Toward understanding their electrochromic behavior Journal of Physical Chemistry C. 120: 9081-9087. DOI: 10.1021/Acs.Jpcc.6B01675 |
0.42 |
|
2015 |
Mallet C, Moussallem C, Faurie A, Allain M, Gohier F, Skene WG, Frère P. Rational Topological Design for Fluorescence Enhancement upon Aggregation of Distyrylfuran Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7944-53. PMID 25868005 DOI: 10.1002/Chem.201500023 |
0.346 |
|
2015 |
Wałęsa-Chorab M, Tremblay MH, Ettaoussi M, Skene WG. Photophysical, electrochemical, and spectroelectrochemical investigation of electronic push-pull benzothiadiazole fluorophores Pure and Applied Chemistry. 87: 649-661. DOI: 10.1515/Pac-2015-0404 |
0.448 |
|
2014 |
Mallet C, Bolduc A, Bishop S, Gautier Y, Skene WG. Unusually high fluorescence quantum yield of a homopolyfluorenylazomethine--towards a universal fluorophore. Physical Chemistry Chemical Physics : Pccp. 16: 24382-90. PMID 25300605 DOI: 10.1039/C4Cp01176G |
0.384 |
|
2014 |
Mulholland ME, Navarathne D, Petrus ML, Dingemans TJ, Skene WG. Correlating on-substrate prepared electrochromes with their solution processed counterparts-towards validating polyazomethines as electrochromes in functioning devices Journal of Materials Chemistry C. 2: 9099-9108. DOI: 10.1039/C4Tc01003E |
0.363 |
|
2014 |
Bolduc A, Barik S, Lenze MR, Meerholz K, Skene WG. Polythiophenoazomethines - Alternate photoactive materials for organic photovoltaics Journal of Materials Chemistry A. 2: 15620-15626. DOI: 10.1039/C4Ta03202K |
0.321 |
|
2014 |
Wałȩsa-Chorab M, Skene WG. On-substrate polymerization-a versatile approach for preparing conjugated polymers suitable as electrochromes and for metal ion sensing Rsc Advances. 4: 19053-19060. DOI: 10.1039/C4Ra00721B |
0.367 |
|
2014 |
Borozenko O, Machado V, Skene WG, Giasson S. Organophosphonic acids as viable linkers for the covalent attachment of polyelectrolyte brushes on silica and mica surfaces Polymer Chemistry. 5: 5740-5750. DOI: 10.1039/C4Py00492B |
0.317 |
|
2014 |
Mulholland ME, Navarathne D, Khedri S, Skene WG. Towards multichromatic electrochromes from ambipolar conjugated azomethines New Journal of Chemistry. 38: 1668-1674. DOI: 10.1039/C4Nj00027G |
0.377 |
|
2014 |
Bolduc A, Skene WG. Direct preparation of electroactive polymers on electrodes and their use in electrochromic devices Polymer Chemistry. 5: 1119-1123. DOI: 10.1039/C3Py01370G |
0.319 |
|
2014 |
Borozenko O, Ou C, Skene WG, Giasson S. Polystyrene-block-poly(acrylic acid) brushes grafted from silica surfaces: PH- and salt-dependent switching studies Polymer Chemistry. 5: 2242-2252. DOI: 10.1039/C3Py01339A |
0.351 |
|
2014 |
Leliège A, Barik S, Skene WG. Photopatternable electrochromic materials from oxetane precursors Acs Applied Materials and Interfaces. 6: 6920-6929. DOI: 10.1021/Am500726N |
0.408 |
|
2014 |
Mbyas Saroukou MS, Skalski T, Skene WG, Lubell WD. Conjugated C3 symmetric aryl tripyrroles and aryl bipyrroles: Synthesis, optical and electronic properties Tetrahedron. 70: 450-458. DOI: 10.1016/J.Tet.2013.11.043 |
0.389 |
|
2013 |
Bolduc A, Dufresne S, Skene WG. The six-membered-ring azomethine N-((E)-{5-[(E)-(pyridin-3-ylimino)methyl]thiophen-2-yl}methylidene)pyridin-3-amine. Acta Crystallographica. Section C, Crystal Structure Communications. 69: 1196-9. PMID 24096515 DOI: 10.1107/S0108270113024566 |
0.367 |
|
2013 |
Fourati MA, Skene WG, Bazuin CG, Prud'homme RE. Photophysical and electrochemical investigations of the fluorescent probe, 4,4'-bis(2-benzoxazolyl)stilbene. The Journal of Physical Chemistry. A. 117: 836-44. PMID 23305534 DOI: 10.1021/Jp312598C |
0.416 |
|
2013 |
Barik S, Navarathne D, Leborgne M, Skene WG. Conjugated thiophenoazomethines: Electrochromic materials exhibiting visible-to-near-IR color changes Journal of Materials Chemistry C. 1: 5508-5519. DOI: 10.1039/C3Tc30494A |
0.389 |
|
2013 |
Mallet C, Le Borgne M, Starck M, Skene WG. Unparalleled fluorescence of a polyazomethine prepared from the self-condensation of an automer and its potential use as a fluorimetric sensor for explosive detection Polymer Chemistry. 4: 250-254. DOI: 10.1039/C2Py20703F |
0.384 |
|
2013 |
Bolduc A, Al Ouahabi A, Mallet C, Skene WG. Insight into the isoelectronic character of azomethines and vinylenes using representative models: A spectroscopic and electrochemical study Journal of Organic Chemistry. 78: 9258-9269. DOI: 10.1021/Jo401497Z |
0.454 |
|
2013 |
Navarathne D, Skene WG. Towards electrochromic devices having visible color switching using electronic push-push and push-pull cinnamaldehyde derivatives Acs Applied Materials and Interfaces. 5: 12646-12653. DOI: 10.1021/Am4040009 |
0.397 |
|
2013 |
Bolduc A, Mallet C, Skene WG. Survey of recent advances of in the field of π-conjugated heterocyclic azomethines as materials with tuneable properties Science China Chemistry. 56: 3-23. DOI: 10.1007/S11426-012-4778-4 |
0.377 |
|
2013 |
Barik S, Skene WG. Turning-on the quenched fluorescence of azomethines through structural modifications European Journal of Organic Chemistry. 2563-2572. DOI: 10.1002/Ejoc.201201502 |
0.399 |
|
2013 |
Sicard L, Navarathne D, Skalski T, Skene WG. On-substrate preparation of an electroactive conjugated polyazomethine from solution-processable monomers and its application in electrochromic devices Advanced Functional Materials. 23: 3549-3559. DOI: 10.1002/Adfm.201203657 |
0.387 |
|
2012 |
Dong Y, Navarathne D, Bolduc A, McGregor N, Skene WG. α,α′-N-boc-substituted Bi- and terthiophenes: Fluorescent precursors for functional materials Journal of Organic Chemistry. 77: 5429-5433. PMID 22606937 DOI: 10.1021/Jo300687D |
0.375 |
|
2012 |
Bolduc A, Knipping E, Skene WG. 2-[(E)-(Pyridin-2-ylmethylidene)amino]thiophene-3-carbonitrile Acta Crystallographica Section E: Structure Reports Online. 68. DOI: 10.1107/S1600536812043188 |
0.329 |
|
2012 |
Bolduc A, Dufresne S, Skene WG. Chemical doping of EDOT azomethine derivatives: Insight into the oxidative and hydrolytic stability Journal of Materials Chemistry. 22: 5053-5064. DOI: 10.1039/C2Jm14248A |
0.422 |
|
2012 |
Bolduc A, Dong Y, Guérin A, Skene WG. Solvatochromic investigation of highly fluorescent 2-aminobithiophene derivatives Physical Chemistry Chemical Physics. 14: 6946-6956. DOI: 10.1039/C2Cp40293A |
0.429 |
|
2012 |
Barik S, Bletzacker T, Skene WG. π-Conjugated fluorescent azomethine copolymers: Opto-electronic, halochromic, and doping properties Macromolecules. 45: 1165-1173. DOI: 10.1021/Ma2024304 |
0.471 |
|
2012 |
Robert P, Bolduc A, Skene WG. Oligofluorenes as polymeric model compounds for providing insight into the triplets of ketone and ketylimine derivatives Journal of Physical Chemistry A. 116: 9305-9314. DOI: 10.1021/Jp307781N |
0.418 |
|
2012 |
Işik D, Santato C, Barik S, Skene WG. Charge-carrier transport in thin films of π-conjugated thiopheno-azomethines Organic Electronics: Physics, Materials, Applications. 13: 3022-3031. DOI: 10.1016/J.Orgel.2012.08.018 |
0.353 |
|
2012 |
Bolduc A, Rivier L, Dufresne S, Skene WG. Spectral investigation of conjugated azomethines: A large palette of colors possible with acid and oxidant doping Materials Chemistry and Physics. 132: 722-728. DOI: 10.1016/J.Matchemphys.2011.12.002 |
0.334 |
|
2012 |
Dufresne S, Skene WG. Optoelectronic property tailoring of conjugated heterocyclic azomethines - The effect of pyrrole, thiophene and furans Journal of Physical Organic Chemistry. 25: 211-221. DOI: 10.1002/Poc.1894 |
0.475 |
|
2011 |
Dufresne S, Bolduc A, Skene WG. Diethyl 2,5-bis-[(2,3-dihydro-thieno[3,4-b][1,4]dioxin-5-yl)methyl-idene-amino]-thio-phene-3,4-dicarboxyl-ate acetone monosolvate. Acta Crystallographica. Section E, Structure Reports Online. 67: o3138. PMID 22199666 DOI: 10.1107/S160053681104339X |
0.351 |
|
2011 |
Dufresne S, Skene WG. Diethyl 2,5-bis-[(1E)-(1H-pyrrol-2-yl-methyl-idene)amino]-thio-phene-3,4-dicarboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 67: o2302. PMID 22058937 DOI: 10.1107/S1600536811031576 |
0.324 |
|
2011 |
Fourati MA, Maris T, Skene WG, Bazuin CG, Prud'homme RE. Photophysical, electrochemical and crystallographic investigations of the fluorophore 2,5-bis(5-tert-butyl-benzoxazol-2-yl)thiophene. The Journal of Physical Chemistry. B. 115: 12362-9. PMID 21916450 DOI: 10.1021/Jp207136K |
0.449 |
|
2011 |
Tshibaka T, Bishop S, Roche IU, Dufresne S, Lubell WD, Skene WG. Conjugated 4-methoxybipyrrole thiophene azomethines: synthesis, opto-electronic properties, and crystallographic characterization. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 10879-88. PMID 21882273 DOI: 10.1002/Chem.201101397 |
0.418 |
|
2011 |
Dufresne S, Skalski T, Skene WG. Insights into the effect of ketylimine, aldimine, and vinylene group attachment and regiosubstitution on the fluorescence deactivation of fluorene Canadian Journal of Chemistry. 89: 173-180. DOI: 10.1139/V10-089 |
0.32 |
|
2011 |
McGregor N, Pardin C, Skene WG. Using quenching kinetics and thermodynamics of amino-fluorophores as empirical tools for predicting boronic acid sensors suitable for use in physiological conditions Australian Journal of Chemistry. 64: 1438-1446. DOI: 10.1071/Ch11297 |
0.345 |
|
2011 |
Barik S, Skene WG. A fluorescent all-fluorene polyazomethine - Towards soluble conjugated polymers exhibiting high fluorescence and electrochromic properties Polymer Chemistry. 2: 1091-1097. DOI: 10.1039/C0Py00394H |
0.46 |
|
2011 |
Dong Y, Bolduc A, McGregor N, Skene WG. Push-pull aminobithiophenes - Highly fluorescent stable fluorophores Organic Letters. 13: 1844-1847. DOI: 10.1021/Ol200353K |
0.386 |
|
2011 |
Borozenko O, Godin R, Lau KL, Mah W, Cosa G, Skene WG, Giasson S. Monitoring in real-time the degrafting of covalently attached fluorescent polymer brushes grafted to silica substrates-effects of pH and salt Macromolecules. 44: 8177-8184. DOI: 10.1021/Ma2013755 |
0.616 |
|
2011 |
Knipping E, Roche IU, Dufresne S, McGregor N, Skene WG. Selective fluorescence turn-on of a prefluorescent azomethine with Zn 2+ Tetrahedron Letters. 52: 4385-4387. DOI: 10.1016/J.Tetlet.2011.06.003 |
0.367 |
|
2011 |
Barik S, Bishop S, Skene WG. Spectroelectrochemical and electrochemical investigation of a highly conjugated all-thiophene polyazomethine Materials Chemistry and Physics. 129: 529-533. DOI: 10.1016/J.Matchemphys.2011.04.060 |
0.415 |
|
2011 |
Tshibaka T, Bishop S, Roche IU, Dufresne S, Lubell WD, Skene WG. Inside Cover: Conjugated 4-Methoxybipyrrole Thiophene Azomethines: Synthesis, Opto-Electronic Properties, and Crystallographic Characterization (Chem. Eur. J. 39/2011) Chemistry - a European Journal. 17: 10786-10786. DOI: 10.1002/Chem.201190191 |
0.311 |
|
2010 |
Dufresne S, Skene WG. Diethyl 2-amino-5-[(E)-(1-methyl-1H-pyrrol-2-yl)methylideneamino]thiophene-3,4-dicarboxylate. Acta Crystallographica. Section E, Structure Reports Online. 66: o3221. PMID 21589512 DOI: 10.1107/S1600536810046775 |
0.332 |
|
2010 |
Dufresne S, Skene WG. Diethyl 2-amino-5-[(E)-(furan-2-yl-methyl-idene)amino]-thio-phene-3,4-di-carboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 66: o3027. PMID 21589183 DOI: 10.1107/S1600536810043746 |
0.338 |
|
2010 |
Barik S, Friedland S, Skene WG. Understanding the reversible anodic behaviour and fluorescence properties of fluorenylazomethines — A structure–property study Canadian Journal of Chemistry. 88: 945-953. DOI: 10.1139/V10-080 |
0.404 |
|
2010 |
Bolduc A, Dufresne S, Hanan GS, Skene WG. Synthesis, photophysics, and electrochemistry of thiophene-pyridine and thiophene-pyrimidine dyad comonomers Canadian Journal of Chemistry. 88: 236-246. DOI: 10.1139/V09-166 |
0.465 |
|
2010 |
Dufresne S, Bolduc A, Skene WG. Towards materials with reversible oxidation and tuneable colours using heterocyclic conjugated azomethines Journal of Materials Chemistry. 20: 4861-4866. DOI: 10.1039/C0Jm00557F |
0.35 |
|
2010 |
Bolduc A, Dufresne S, Skene WG. EDOT-containing azomethine: An easily prepared electrochromically active material with tuneable colours Journal of Materials Chemistry. 20: 4820-4826. DOI: 10.1039/B923821B |
0.362 |
|
2010 |
Lego B, Skene WG, Giasson S. Swelling study of responsive polyelectrolyte brushes grafted from mica substrates: Effect of pH, salt, and grafting density Macromolecules. 43: 4384-4393. DOI: 10.1021/Ma902588J |
0.336 |
|
2010 |
Barik S, Skene WG. Selective chain-end postpolymerization reactions and property tuning of a highly conjugated and all-thiophene polyazomethine Macromolecules. 43: 10435-10441. DOI: 10.1021/Ma102245P |
0.379 |
|
2010 |
Dufresne S, Roche IU, Skalski T, Skene WG. Insights into the effect of the ketylimine group on the fluorescence deactivation of oligofluorenes Journal of Physical Chemistry C. 114: 13106-13112. DOI: 10.1021/Jp104026Y |
0.428 |
|
2010 |
Bolduc A, Lachapelle V, Skene WG. Snap together bonds for amine capturing - New spectroscopic and amperometric sensors Macromolecular Symposia. 297: 87-93. DOI: 10.1002/Masy.200900065 |
0.438 |
|
2010 |
Lego B, Skene WG, Giasson S. Neutral and charged brushes covalently grafted from OH-functionalized mica surfaces using surface-initiated ATRP - Swelling investigation by AFM Macromolecular Symposia. 297: 65-68. DOI: 10.1002/Masy.200900063 |
0.313 |
|
2010 |
Borozenko O, Skene WG, Giasson S. Direct Polymerization of Polyacrylic Acid on Mica Substrates using ATRP - A Preliminary Study Macromolecular Symposia. 297: 1-5. DOI: 10.1002/Masy.200900056 |
0.314 |
|
2009 |
Dufresne S, Callaghan L, Skene WG. Conjugated fluorenes prepared from azomethines connections--II: The effect of alternating fluorenones and fluorenes on the spectroscopic and electrochemical properties. The Journal of Physical Chemistry. B. 113: 15541-9. PMID 19921952 DOI: 10.1021/Jp907391Y |
0.401 |
|
2009 |
Tshibaka T, Ulliel Roche I, Dufresne S, Lubell WD, Skene WG. Unsymmetric electronic push-pull bipyrroles - synthesis, spectroelectrochemical, and photophysical investigation. The Journal of Organic Chemistry. 74: 9497-500. PMID 19911772 DOI: 10.1021/Jo901965T |
0.345 |
|
2009 |
Dufresne S, Pérez Guarìn SA, Bolduc A, Bourque AN, Skene WG. Conjugated fluorene-thiophenes prepared from azomethine connections. Part I. The effect of electronic and aryl groups on the spectroscopic and electrochemical properties. Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society For Photobiology. 8: 796-804. PMID 19492107 DOI: 10.1039/B819735K |
0.455 |
|
2009 |
Lego B, François M, Skene WG, Giasson S. Polymer brush covalently attached to OH-functionalized mica surface via surface-initiated ATRP: control of grafting density and polymer chain length. Langmuir : the Acs Journal of Surfaces and Colloids. 25: 5313-21. PMID 19256467 DOI: 10.1021/La804060S |
0.331 |
|
2009 |
Bourque AN, Dufresne S, Skene WG. Thiophene-phenyl azomethines with varying rotational barriers-model compounds for examining imine fluorescence deactivation Journal of Physical Chemistry C. 113: 19677-19685. DOI: 10.1021/Jp907263P |
0.432 |
|
2008 |
Dufresne S, Skene WG. Diethyl 2-[(1-methyl-1H-pyrrol-2-yl)methyl-ene-amino]-5-(2-thienylmethyl-ene-amino)thio-phene-3,4-dicarboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 64: o782. PMID 21202275 DOI: 10.1107/S160053680800799X |
0.335 |
|
2008 |
Dufresne S, Skene WG. Diethyl 2,5-bis-[(E)-2-furylmethyl-ene-amino]thio-phene-3,4-dicarboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 64: o710. PMID 21202101 DOI: 10.1107/S1600536808006612 |
0.313 |
|
2008 |
Dufresne S, Skene WG. Unsymmetric pyrrole, thiophene, and furan-conjugated comonomers prepared using azomethine connections: potential new monomers for alternating homocoupled products. The Journal of Organic Chemistry. 73: 3859-66. PMID 18410143 DOI: 10.1021/Jo8002503 |
0.424 |
|
2008 |
Lego B, Skene WG, Giasson S. Unprecedented covalently attached ATRP initiator onto OH-functionalized mica surfaces. Langmuir : the Acs Journal of Surfaces and Colloids. 24: 379-82. PMID 18076200 DOI: 10.1021/La703051B |
0.33 |
|
2008 |
Dufresne S, Gaultois M, Skene WG. Environmentally friendly preparation of a conjugated polyazostilbene: A photophysical and electrochemical investigation Optical Materials. 30: 961-967. DOI: 10.1016/J.Optmat.2007.05.031 |
0.41 |
|
2007 |
Dufresne S, Bourque AN, Skene WG. (E)-5-(2-Thienylmethyl-eneamino)quinolin-8-ol. Acta Crystallographica. Section E, Structure Reports Online. 64: o316. PMID 21200877 DOI: 10.1107/S1600536807066652 |
0.337 |
|
2007 |
Bourgeaux M, Skene WG. Photophysics and electrochemistry of conjugated oligothiophenes prepared by using azomethine connections Journal of Organic Chemistry. 72: 8882-8892. PMID 17956121 DOI: 10.1021/Jo701515J |
0.476 |
|
2007 |
Guy J, Caron K, Dufresne S, Michnick SW, Skene WG, Keillor JW. Convergent preparation and photophysical characterization of dimaleimide dansyl fluorogens: elucidation of the maleimide fluorescence quenching mechanism. Journal of the American Chemical Society. 129: 11969-77. PMID 17850081 DOI: 10.1021/Ja0738125 |
0.395 |
|
2007 |
Dufresne S, Hanan GS, Skene WG. Preparation, photophysics, and electrochemistry of segmented comonomers consisting of thiophene and pyrimidine units: new monomers for hybrid copolymers. The Journal of Physical Chemistry. B. 111: 11407-18. PMID 17845027 DOI: 10.1021/Jp075259J |
0.686 |
|
2007 |
Dufresne S, Pérez Guarìn SA, Skene WG. A fluoresceinophane: 1(9),4,16-trioxa-1(2,10)-anthracena-2(1,2)-benzenacyclohexadecaphane-1(7),3(1(9)H)-dione. Acta Crystallographica. Section C, Crystal Structure Communications. 63: o350-2. PMID 17551201 DOI: 10.1107/S0108270107008566 |
0.36 |
|
2007 |
Guarìn SA, Bourgeaux M, Dufresne S, Skene WG. Photophysical, crystallographic, and electrochemical characterization of symmetric and unsymmetric self-assembled conjugated thiopheno azomethines. The Journal of Organic Chemistry. 72: 2631-43. PMID 17343421 DOI: 10.1021/Jo070100O |
0.472 |
|
2007 |
Dufresne S, Gaultois M, Skene WG. Disodium 5,5′-diamino-2,2′-ethyl-enedibenzene-sulfonate tetra-hydrate Acta Crystallographica Section E: Structure Reports Online. 63. DOI: 10.1107/S1600536807049410 |
0.349 |
|
2007 |
Dufresne S, Gaultois M, Skene WG. Bis(triethylammonium) 4,4′-diamino-trans-stilbene-2,2′- disulfonate Acta Crystallographica Section E: Structure Reports Online. 63. DOI: 10.1107/S1600536807041360 |
0.364 |
|
2007 |
Bourgeaux M, Skene WG. Ethyl 2-aminothiophene-3-carboxylate Acta Crystallographica Section E: Structure Reports Online. 63. DOI: 10.1107/S1600536807009683 |
0.326 |
|
2007 |
Guarìn SAP, Dufresne S, Tsang D, Sylla A, Skene WG. Photophysical, electrochemical, and crystallographic investigation of conjugated fluoreno azomethines and their precursors Journal of Materials Chemistry. 17: 2801-2811. DOI: 10.1039/B618098A |
0.44 |
|
2007 |
Dufresne S, Bourgeaux M, Skene WG. Tunable spectroscopic and electrochemical properties of conjugated push-push, push-pull and pull-pull thiopheno azomethines Journal of Materials Chemistry. 17: 1166-1177. DOI: 10.1039/B616379C |
0.44 |
|
2007 |
Bourgeaux M, Guarìn SAP, Skene WG. Photophysical, crystallographic, and electrochemical characterization of novel conjugated thiopheno azomethines Journal of Materials Chemistry. 17: 972-979. DOI: 10.1039/B615325A |
0.444 |
|
2007 |
Pérez Guarìn SA, Tsang D, Skene WG. Spectroscopic studies of a fluorescent fluoresceinophane formed via a practical synthetic route New Journal of Chemistry. 31: 210-217. DOI: 10.1039/B611060F |
0.409 |
|
2007 |
Bourgeaux M, Skene WG. A highly conjugated p- and n-type polythiophenoazomethine: Synthesis, spectroscopic, and electrochemical investigation Macromolecules. 40: 1792-1795. DOI: 10.1021/Ma070292P |
0.388 |
|
2007 |
Ioachim E, Medlycott EA, Skene WG, Hanan GS. Synthesis and properties of 6,6′-dithienyl-4,4′-bipyrimidine and its hetero- and homo-leptic Ru(II) complexes Polyhedron. 26: 4929-4935. DOI: 10.1016/J.Poly.2007.06.025 |
0.304 |
|
2007 |
Pérez Guarìn SA, Skene WG. Thermal, photophysical, and electrochemical characterization of a conjugated polyazomethine prepared by anodic electropolymerization of a thiophenoazomethine co-monomer Materials Letters. 61: 5102-5106. DOI: 10.1016/J.Matlet.2007.04.015 |
0.414 |
|
2007 |
Tsang D, Bourgeaux M, Skene WG. Demystifying the triplet state and the quenching mechanism of self-assembled fluorenoazomethines Journal of Photochemistry and Photobiology a: Chemistry. 192: 122-129. DOI: 10.1016/J.Jphotochem.2007.05.013 |
0.406 |
|
2007 |
Skene WG, Pérez Guarìn SA. Spectral characterization of thiophene acylhydrazides Journal of Fluorescence. 17: 540-546. DOI: 10.1007/S10895-007-0209-X |
0.402 |
|
2006 |
Skene WG, Berl V, Risler H, Khoury R, Lehn JM. Selective product amplification of thymine photodimer by recognition-directed supramolecular assistance Organic and Biomolecular Chemistry. 4: 3652-3663. PMID 16990941 DOI: 10.1039/B605658J |
0.475 |
|
2006 |
Dufresne S, Bourgeaux M, Skene WG. Diethyl 2,5-bis[(E)-thiophen-2-ylmethyleneamino]-thiophene-3,4- dicarboxylate Acta Crystallographica Section E: Structure Reports Online. 62. DOI: 10.1107/S1600536806046915 |
0.349 |
|
2006 |
Bourgeaux M, Vomsheid S, Skene WG. Hydrogen-bonded network of diethyl 2,5-diaminothiophene-3,4-dicarboxylate Acta Crystallographica Section E: Structure Reports Online. 62. DOI: 10.1107/S160053680604606X |
0.309 |
|
2006 |
Skene WG, Dufresne S, Trefz T, Simard M. (E)-Diethyl 2-amino-5-(2-thienylmethyleneamino)thiophene-3,4-dicarboxylate Acta Crystallographica Section E: Structure Reports Online. 62: o2382-o2384. DOI: 10.1107/S1600536806017351 |
0.33 |
|
2006 |
Skene WG, Dufresne S. A naphthalene-thiophene-naphthalene diazomethine triad solvated with dichloromethane Acta Crystallographica Section E: Structure Reports Online. 62. DOI: 10.1107/S1600536806005411 |
0.342 |
|
2005 |
Hansford KA, Perez Guarin SA, Skene WG, Lubell WD. Bis(pyrrol-2-yl)arylenes from the tandem bidirectional addition of vinyl Grignard reagent to aryl diesters. The Journal of Organic Chemistry. 70: 7996-8000. PMID 16277320 DOI: 10.1021/Jo0510888 |
0.347 |
|
2004 |
Skene WG, Dufresne S. Easy one-pot synthesis of energy transfer cassettes. Organic Letters. 6: 2949-52. PMID 15330655 DOI: 10.1021/Ol048977M |
0.308 |
|
2003 |
Skene WG, Couzigné E, Lehn JM. Supramolecular control of the template-induced selective photodimerization of 4-methyl-7-O-hexylcoumarin. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 5560-6. PMID 14639639 DOI: 10.1002/Chem.200305268 |
0.462 |
|
2000 |
Skene WG, Scaiano JC, Yap GPA. Improved mimetic compound for styrene `living' free radical polymerization. An initiator containing the `penultimate' unit Macromolecules. 33: 3536-3542. DOI: 10.1021/Ma991924D |
0.408 |
|
2000 |
Skene WG, Scaiano JC, Listigovers NA, Kazmaier PM, Georges MK. Rate constants for the trapping of various carbon-centered radicals by nitroxides: unimolecular initiators for living free radical polymerization Macromolecules. 33: 5065-5072. DOI: 10.1021/Ma991753C |
0.459 |
|
2000 |
Skene WG, Connolly TJ, Scaiano JC. Trapping of photogenerated group IV radicals by TEMPO: Potential new organometallic initiators for ?living? free radical polymerization International Journal of Chemical Kinetics. 32: 238-244. DOI: 10.1002/(Sici)1097-4601(2000)32:4<238::Aid-Kin6>3.0.Co;2-A |
0.443 |
|
2000 |
Skene WG, Scaiano JC. Photoinduced TEMPO release from a living free radical polymerization initiator American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. 41: 163-164. |
0.485 |
|
1999 |
Skene WG, Connolly TJ, Scaiano JC. The thermolysis and photochemistry of hybrid initiators for 'living' free radical polymerization Tetrahedron Letters. 40: 7297-7302. DOI: 10.1016/S0040-4039(99)01372-6 |
0.47 |
|
1998 |
Skene WG, Belt ST, Connolly TJ, Hahn P, Scaiano JC. Decomposition Kinetics, Arrhenius Parameters, and Bond Dissociation Energies for Alkoxyamines of Relevance in “Living” Free Radical Polymerization Macromolecules. 31: 9103-9105. DOI: 10.1021/Ma9812229 |
0.463 |
|
1996 |
Skene WG, Scaiano JC, Cozens FL. Fluorescence from Samarium(II) Iodide and Its Electron Transfer Quenching: Dynamics of the Reaction of Benzyl Radicals with Sm(II). The Journal of Organic Chemistry. 61: 7918-7921. PMID 11667752 DOI: 10.1021/Jo960473H |
0.48 |
|
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