| Year |
Citation |
Score |
| 2020 |
Bukuroshi E, Petersen AU, Broløs L, Bender TP, Nielsen MB. Exploring the Synthesis and Electronic Properties of Axially Substituted Boron Subphthalocyanines with Carbon‐based Functional Groups European Journal of Inorganic Chemistry. DOI: 10.1002/Ejic.202000525 |
0.322 |
|
| 2019 |
Grant TM, Josey DS, Sampson KL, Mudigonda T, Bender TP, Lessard BH. Boron Subphthalocyanines and Silicon Phthalocyanines for Use as Active Materials in Organic Photovoltaics. Chemical Record (New York, N.Y.). PMID 30672126 DOI: 10.1002/Tcr.201800178 |
0.363 |
|
| 2019 |
Kamino BA, Szawiola AM, Plint T, Bender TP. Formation and application of electrochemically active cross-linked triarylamine–siloxane films using the Piers–Rubinsztajn reaction Canadian Journal of Chemistry. 97: 378-386. DOI: 10.1139/Cjc-2018-0071 |
0.312 |
|
| 2018 |
Garner RK, Josey DS, Nyikos SR, Dovijarski A, Wang JM, Evans GJ, Bender TP. Boron subphthalocyanines as electron donors in outdoor lifetime monitored organic photovoltaic cells Solar Energy Materials and Solar Cells. 176: 331-335. DOI: 10.1016/J.Solmat.2017.10.018 |
0.382 |
|
| 2018 |
Plint TG, Lessard BH, Bender TP. Doping chloro boron subnaphthalocyanines and chloro boron subphthalocyanine in simple OLED architectures yields warm white incandescent-like emissions Optical Materials. 75: 710-718. DOI: 10.1016/J.Optmat.2017.11.028 |
0.334 |
|
| 2017 |
Sampson KL, Lessard BH, Cho E, Bender TP. Boron Subphthalocyanine Coupled to Methacrylate-Rich Terpolymers by Nitroxide Mediated Polymerization: The Subphthalocyanine Dictates the Phase Transition Temperatures Macromolecular Chemistry and Physics. 218: 1600592. DOI: 10.1002/Macp.201600592 |
0.323 |
|
| 2016 |
Lessard BH, Lough AJ, Bender TP. Crystal structures of bis-(phen-oxy)silicon phthalocyanines: increasing π-π inter-actions, solubility and disorder and no halogen bonding observed. Acta Crystallographica. Section E, Crystallographic Communications. 72: 988-94. PMID 27555947 DOI: 10.1107/S205698901600935X |
0.34 |
|
| 2016 |
Castrucci JS, Garner RK, Dang JD, Thibau E, Lu ZH, Bender TP. Characterization of μ-oxo-(BsubPc)2 in Multiple Organic Photovoltaic Device Architectures: Comparing Against and Combining with Cl-BsubPc. Acs Applied Materials & Interfaces. PMID 27548372 DOI: 10.1021/Acsami.6B06717 |
0.373 |
|
| 2016 |
Lessard BH, Dang JD, Grant TM, Gao D, Seferos DS, Bender TP. Correction to Bis(trin-hexylsilyl oxide) Silicon Phthalocyanine: A Unique Additive in Ternary Bulk Heterojunction Organic Photovoltaic Devices. Acs Applied Materials & Interfaces. PMID 27459000 DOI: 10.1021/Acsami.6B06902 |
0.318 |
|
| 2016 |
Virdo JD, Lough AJ, Bender TP. Redetermination of the crystal structure of boron subphthalocyanine chloride (Cl-BsubPc) enabled by slow train sublimation. Acta Crystallographica. Section C, Structural Chemistry. 72: 297-307. PMID 27045180 DOI: 10.1107/S2053229616003491 |
0.349 |
|
| 2016 |
Plint T, Lessard BH, Bender TP. Assessing the potential of group 13 and 14 metal/metalloid phthalocyanines as hole transport layers in organic light emitting diodes Journal of Applied Physics. 119. DOI: 10.1063/1.4945377 |
0.33 |
|
| 2016 |
Dang JD, Josey DS, Lough AJ, Li Y, Sifate A, Lu ZH, Bender TP. The mixed alloyed chemical composition of chloro-(chloro):N-boron subnaphthalocyanines dictates their physical properties and performance in organic photovoltaic devices Journal of Materials Chemistry A. 4: 9566-9577. DOI: 10.1039/C6Ta02457B |
0.352 |
|
| 2015 |
Bonnier C, Bender TP. Ring Opening Reactions through C-O Bond Cleavage Uniquely Adding Chemical Functionality to Boron Subphthalocyanine. Molecules (Basel, Switzerland). 20: 18237-45. PMID 26457699 DOI: 10.3390/Molecules201018237 |
0.338 |
|
| 2015 |
Castrucci JS, Josey DS, Thibau E, Lu ZH, Bender TP. Boron Subphthalocyanines as Triplet Harvesting Materials within Organic Photovoltaics. The Journal of Physical Chemistry Letters. 6: 3121-5. PMID 26267212 DOI: 10.1021/Acs.Jpclett.5B01254 |
0.36 |
|
| 2015 |
Melville OA, Lessard BH, Bender TP. Phthalocyanine-Based Organic Thin-Film Transistors: A Review of Recent Advances. Acs Applied Materials & Interfaces. 7: 13105-18. PMID 26000612 DOI: 10.1021/Acsami.5B01718 |
0.344 |
|
| 2015 |
Josey DS, Castrucci JS, Dang JD, Lessard BH, Bender TP. Evaluating thiophene electron-donor layers for the rapid assessment of boron subphthalocyanines as electron acceptors in organic photovoltaics: solution or vacuum deposition? Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 16: 1245-50. PMID 25765007 DOI: 10.1002/Cphc.201402751 |
0.347 |
|
| 2015 |
Lessard BH, White RT, Al-Amar M, Plint T, Castrucci JS, Josey DS, Lu ZH, Bender TP. Assessing the potential roles of silicon and germanium phthalocyanines in planar heterojunction organic photovoltaic devices and how pentafluoro phenoxylation can enhance π-π interactions and device performance. Acs Applied Materials & Interfaces. 7: 5076-88. PMID 25665015 DOI: 10.1021/Am508491V |
0.341 |
|
| 2015 |
Dang JD, Fulford MV, Kamino BA, Paton AS, Bender TP. Process for the synthesis of symmetric and unsymmetric oxygen bridged dimers of boron subphthalocyanines (μ-oxo-(BsubPc)2s). Dalton Transactions (Cambridge, England : 2003). 44: 4280-8. PMID 25632928 DOI: 10.1039/C4Dt02624A |
0.353 |
|
| 2015 |
Bonnier C, Josey DS, Bender TP. Aryl-Substituted boron subphthalocyanines and their application in organic photovoltaics Australian Journal of Chemistry. 68: 1750-1758. DOI: 10.1071/Ch15381 |
0.378 |
|
| 2015 |
Lessard BH, Grant TM, White R, Thibau E, Lu ZH, Bender TP. The position and frequency of fluorine atoms changes the electron donor/acceptor properties of fluorophenoxy silicon phthalocyanines within organic photovoltaic devices Journal of Materials Chemistry A. 3: 24512-24524. DOI: 10.1039/C5Ta07173A |
0.421 |
|
| 2015 |
Raboui H, Al-Amar M, Abdelrahman AI, Bender TP. Axially phenoxylated aluminum phthalocyanines and their application in organic photovoltaic cells Rsc Advances. 5: 45731-45739. DOI: 10.1039/C5Ra04919A |
0.661 |
|
| 2015 |
Lessard BH, Al-Amar M, Grant TM, White R, Lu ZH, Bender TP. From chloro to fluoro, expanding the role of aluminum phthalocyanine in organic photovoltaic devices Journal of Materials Chemistry A. 3: 5047-5053. DOI: 10.1039/C4Ta06759B |
0.351 |
|
| 2015 |
Plint TG, Kamino BA, Bender TP. Charge carrier mobility of siliconized liquid triarylamine organic semiconductors by time-of-flight spectroscopy Journal of Physical Chemistry C. 119: 1676-1682. DOI: 10.1021/Jp510474B |
0.311 |
|
| 2015 |
Lessard BH, Sampson KL, Plint T, Bender TP. Boron subphthalocyanine polymers: Avoiding the small molecule side product and exploring their use in organic light-emitting diodes Journal of Polymer Science, Part a: Polymer Chemistry. 53: 1996-2006. DOI: 10.1002/Pola.27685 |
0.35 |
|
| 2014 |
Lessard BH, Dang JD, Grant TM, Gao D, Seferos DS, Bender TP. Bis(tri-n-hexylsilyl oxide) silicon phthalocyanine: a unique additive in ternary bulk heterojunction organic photovoltaic devices. Acs Applied Materials & Interfaces. 6: 15040-51. PMID 25105425 DOI: 10.1021/Am503038T |
0.33 |
|
| 2014 |
Morse GE, Gantz JL, Steirer KX, Armstrong NR, Bender TP. Pentafluorophenoxy boron subphthalocyanine (F5BsubPc) as a multifunctional material for organic photovoltaics. Acs Applied Materials & Interfaces. 6: 1515-24. PMID 24372192 DOI: 10.1021/Am404179Z |
0.336 |
|
| 2014 |
Paton AS, Bender TP. Some observations regarding the behavior of boron subphthalocyanines in polar aprotic solvents Journal of Porphyrins and Phthalocyanines. 18: 1051-1056. DOI: 10.1142/S1088424614500886 |
0.321 |
|
| 2014 |
Beaumont N, Castrucci JS, Sullivan P, Morse GE, Paton AS, Lu ZH, Bender TP, Jones TS. Acceptor properties of boron subphthalocyanines in fullerene free photovoltaics Journal of Physical Chemistry C. 118: 14813-14823. DOI: 10.1021/Jp503578G |
0.382 |
|
| 2014 |
Morse GE, Gong I, Kawar Y, Lough AJ, Bender TP. Crystal and solid-state arrangement trends of halogenated boron subphthalocyanines Crystal Growth and Design. 14: 2138-2147. DOI: 10.1021/Cg401475B |
0.326 |
|
| 2014 |
Castrucci JS, Dang JD, Kamino BA, Campbell A, Pitts D, Lu ZH, Bender TP. Considerations for the physical vapor deposition of high molar mass organic compounds Vacuum. 109: 26-33. DOI: 10.1016/J.Vacuum.2014.05.023 |
0.333 |
|
| 2013 |
Kamino BA, Bender TP. Modified boron subphthalocyanines with stable electrochemistry and tuneable bandgaps. Dalton Transactions (Cambridge, England : 2003). 42: 13145-50. PMID 23880986 DOI: 10.1039/C3Dt50615K |
0.306 |
|
| 2013 |
Kamino BA, Bender TP. The use of siloxanes, silsesquioxanes, and silicones in organic semiconducting materials. Chemical Society Reviews. 42: 5119-30. PMID 23549525 DOI: 10.1039/C3Cs35519E |
0.36 |
|
| 2013 |
Lessard BH, Bender TP. Boron subphthalocyanine polymers by facile coupling to poly(acrylic acid-ran-styrene) copolymers synthesized by nitroxide-mediated polymerization and the associated problems with autoinitiation. Macromolecular Rapid Communications. 34: 568-73. PMID 23386322 DOI: 10.1002/Marc.201200787 |
0.366 |
|
| 2013 |
Virdo JD, Kawar YH, Lough AJ, Bender TP. Halogen bonds can direct the solid state arrangement of phenoxy-boron subphthalocyanines Crystengcomm. 15: 3187-3199. DOI: 10.1039/C3Ce26711C |
0.312 |
|
| 2013 |
Paton AS, Morse GE, Lough AJ, Bender TP. Utilizing the π-acidity of boron subphthalocyanine to achieve novel solid-state arrangements Crystal Growth and Design. 13: 5368-5374. DOI: 10.1021/Cg4012795 |
0.358 |
|
| 2013 |
Gretton MJ, Kamino BA, Bender TP. Extension of the application of piers-rubinsztajn conditions to produce triarylamine pendant dimethylsiloxane copolymers Macromolecular Symposia. 324: 82-94. DOI: 10.1002/Masy.201200071 |
0.344 |
|
| 2012 |
Kamino BA, Bender TP, Klenkler RA. Hole Mobility of a Liquid Organic Semiconductor. The Journal of Physical Chemistry Letters. 3: 1002-6. PMID 26286563 DOI: 10.1021/Jz300058W |
0.314 |
|
| 2012 |
Fulford MV, Lough AJ, Bender TP. The first report of the crystal structure of non-solvated μ-oxo boron subphthalocyanine and the crystal structures of two solvated forms. Acta Crystallographica. Section B, Structural Science. 68: 636-45. PMID 23165600 DOI: 10.1107/S0108768112037184 |
0.315 |
|
| 2012 |
Paton AS, Lough AJ, Bender TP. Sulfonate pseudohalides of boron subphthalocyanine. Acta Crystallographica. Section C, Crystal Structure Communications. 68: o459-64. PMID 23124463 DOI: 10.1107/S0108270112040425 |
0.321 |
|
| 2012 |
Sepehrifard A, Kamino BA, Bender TP, Morin S. Siliconized triarylamines as redox mediator in dye-sensitized solar cells. Acs Applied Materials & Interfaces. 4: 6211-5. PMID 23113755 DOI: 10.1021/Am301812D |
0.335 |
|
| 2012 |
Morse GE, Bender TP. Boron subphthalocyanines as organic electronic materials. Acs Applied Materials & Interfaces. 4: 5055-68. PMID 22979940 DOI: 10.1021/Am3015197 |
0.356 |
|
| 2012 |
Morse GE, Bender TP. Aluminum chloride activation of chloro-boronsubphthalocyanine: a rapid and flexible method for axial functionalization with an expanded set of nucleophiles. Inorganic Chemistry. 51: 6460-7. PMID 22642220 DOI: 10.1021/Ic2016935 |
0.324 |
|
| 2012 |
Kamino BA, Mills B, Reali C, Gretton MJ, Brook MA, Bender TP. Liquid triarylamines: the scope and limitations of Piers-Rubinsztajn conditions for obtaining triarylamine-siloxane hybrid materials. The Journal of Organic Chemistry. 77: 1663-74. PMID 22220839 DOI: 10.1021/Jo2020906 |
0.354 |
|
| 2012 |
Dang JD, Virdo JD, Lessard BH, Bultz E, Paton AS, Bender TP. A boron subphthalocyanine polymer: Poly(4-methylstyrene)-co-poly(phenoxy boron subphthalocyanine) Macromolecules. 45: 7791-7798. DOI: 10.1021/Ma301247P |
0.35 |
|
| 2012 |
Gretton MJ, Kamino BA, Brook MA, Bender TP. The use of Piers-Rubinsztajn conditions for the placement of triarylamines pendant to silicone polymers Macromolecules. 45: 723-728. DOI: 10.1021/Ma202041U |
0.306 |
|
| 2012 |
Fulford MV, Jaidka D, Paton AS, Morse GE, Brisson ERL, Lough AJ, Bender TP. Crystal structures, reaction rates, and selected physical properties of halo-boronsubphthalocyanines (Halo = Fluoride, chloride, and bromide) Journal of Chemical and Engineering Data. 57: 2756-2765. DOI: 10.1021/Je3005112 |
0.329 |
|
| 2012 |
Paton AS, Lough AJ, Bender TP. One well-placed methyl group increases the solubility of phenoxy boronsubphthalocyanine two orders of magnitude Industrial and Engineering Chemistry Research. 51: 6290-6296. DOI: 10.1021/Ie202998F |
0.378 |
|
| 2012 |
Castrucci JS, Helander MG, Morse GE, Lu ZH, Yip CM, Bender TP. Charge carrier mobility in fluorinated phenoxy boron subphthalocyanines: Role of solid state packing Crystal Growth and Design. 12: 1095-1100. DOI: 10.1021/Cg2015385 |
0.329 |
|
| 2012 |
Grande JB, Fawcett AS, McLaughlin AJ, Gonzaga F, Bender TP, Brook MA. Anhydrous formation of foamed silicone elastomers using the Piers-Rubinsztajn reaction Polymer (United Kingdom). 53: 3135-3142. DOI: 10.1016/J.Polymer.2012.05.033 |
0.333 |
|
| 2012 |
Kamino BA, Chang YL, Lu ZH, Bender TP. Phthalonitrile based fluorophores as fluorescent dopant emitters in deep-blue OLEDs: Approaching the NTSC standard for blue Organic Electronics: Physics, Materials, Applications. 13: 1479-1485. DOI: 10.1016/J.Orgel.2012.04.014 |
0.304 |
|
| 2011 |
Morse GE, Castrucci JS, Helander MG, Lu ZH, Bender TP. Phthalimido-boronsubphthalocyanines: new derivatives of boronsubphthalocyanine with bipolar electrochemistry and functionality in OLEDs. Acs Applied Materials & Interfaces. 3: 3538-44. PMID 21812440 DOI: 10.1021/Am200758W |
0.348 |
|
| 2011 |
Kamino BA, Grande JB, Brook MA, Bender TP. Siloxane-triarylamine hybrids: discrete room temperature liquid triarylamines via the Piers-Rubinsztajn reaction. Organic Letters. 13: 154-7. PMID 21128649 DOI: 10.1021/Ol102607V |
0.309 |
|
| 2011 |
Paton AS, Lough AJ, Bender TP. A role for π-Br interactions in the solid-state molecular packing of para-halo-phenoxy-boronsubphthalocyanines Crystengcomm. 13: 3653-3656. DOI: 10.1039/C0Ce00796J |
0.321 |
|
| 2011 |
Paton AS, Morse GE, Lough AJ, Bender TP. Observations regarding the crystal structures of non-halogenated phenoxyboronsubphthalocyanines having para substituents on the phenoxy group Crystengcomm. 13: 914-919. DOI: 10.1039/C0Ce00599A |
0.352 |
|
| 2011 |
Kamino BA, Morse GE, Bender TP. Effect of triarylamine structure on the photoinduced electron transfer to boron subphthalocyanine Journal of Physical Chemistry C. 115: 20716-20723. DOI: 10.1021/Jp206259S |
0.331 |
|
| 2011 |
Brisson ERL, Paton AS, Morse GE, Bender TP. Boron subphthalocyanine dyes: 3-pentadecylphenol as a solubilizing molecular fragment Industrial and Engineering Chemistry Research. 50: 10910-10917. DOI: 10.1021/Ie200480X |
0.347 |
|
| 2011 |
Kamino BA, Castrucci J, Bender TP. Controlling the Physical and Electrochemical Properties of Arylamines Through the Use of Simple Silyl Ethers: Liquid, Waxy and Glassy Arylamines Silicon. 3: 125-137. DOI: 10.1007/S12633-011-9088-5 |
0.351 |
|
| 2010 |
Morse GE, Maka JF, Lough AJ, Bender TP. Bromido(dodecafluorosubphthalo-cyaninato)boron(III). Acta Crystallographica. Section E, Structure Reports Online. 66: o3057-8. PMID 21589368 DOI: 10.1107/S1600536810041863 |
0.315 |
|
| 2010 |
Morse GE, Paton AS, Lough A, Bender TP. Chloro boron subphthalocyanine and its derivatives: dyes, pigments or somewhere in between? Dalton Transactions (Cambridge, England : 2003). 39: 3915-22. PMID 20372716 DOI: 10.1039/B922199A |
0.331 |
|
| 2010 |
Morse GE, Helander MG, Maka JF, Lu ZH, Bender TP. Fluorinated phenoxy boron subphthalocyanines in organic light-emitting diodes Acs Applied Materials and Interfaces. 2: 1934-1944. DOI: 10.1021/Am1002603 |
0.357 |
|
| 2007 |
McNulty J, Cheekoori S, Bender TP, Coggan JA. A Pronounced Anionic Effect in the Pd-Catalyzed Buchwald—Hartwig Amination Reaction Revealed in Phosphonium Salt Ionic Liquids. Cheminform. 38. DOI: 10.1002/Ejoc.200700005 |
0.301 |
|
| 2002 |
Bender TP, Burt RA, Hamer GK, DeVisser C, Smith PF, Saban M. The synthesis of poly(arylene ether)s in solution at pilot-plant scale with control over molecular weight and end-group composition Organic Process Research and Development. 6: 714-720. DOI: 10.1021/Op025519P |
0.308 |
|
| 2001 |
Bender TP, Graham JF, Duff JM. Effect of Substitution on the Electrochemical and Xerographic Properties of Triarylamines: Correlation to the Hammett Parameter of the Substituent and Calculated HOMO Energy Level Chemistry of Materials. 13: 4105-4111. DOI: 10.1021/Cm010281P |
0.32 |
|
| 2000 |
Wang ZY, Bender TP, Zheng HB, Chen LZ. Molecular approach to the development of polyimides with novel structures and properties Polymers For Advanced Technologies. 11: 652-657. DOI: 10.1002/1099-1581(200008/12)11:8/12<652::Aid-Pat16>3.0.Co;2-2 |
0.354 |
|
| 2000 |
Bender TP, Wang ZY. Synthesis of polyimides and segmented block copolyimides by transimidization Journal of Polymer Science Part a: Polymer Chemistry. 38: 3991-3996. DOI: 10.1002/1099-0518(20001101)38:21<3991::Aid-Pola170>3.0.Co;2-Y |
0.335 |
|
| 2000 |
Bender TP, MacKinnon SM, Wang ZY. Poly(aryl ether)s containingo-terphenyl subunits. III. Random copoly(ether imide)s Journal of Polymer Science Part a: Polymer Chemistry. 38: 758-763. DOI: 10.1002/(Sici)1099-0518(20000215)38:4<758::Aid-Pola11>3.0.Co;2-M |
0.325 |
|
| 2000 |
Mackinnon SM, Bender TP, Wang ZY. Poly(aryl ether)s containingo-terphenyl subunits. II. Random poly(ether sulfone)s Journal of Polymer Science Part a: Polymer Chemistry. 38: 9-17. DOI: 10.1002/(Sici)1099-0518(20000101)38:1<9::Aid-Pola2>3.0.Co;2-8 |
0.345 |
|
| 1998 |
Bender TP, Wang ZY. Soluble alternating copolyimides containing the tetrahydro[5]helicene unit Journal of Polymer Science Part a: Polymer Chemistry. 36: 1349-1353. DOI: 10.1002/(Sici)1099-0518(19980715)36:9<1349::Aid-Pola1>3.0.Co;2-O |
0.311 |
|
| 1997 |
Wang ZY, Qi Y, Bender TP, Gao JP. Condensation Polyimides from AB-Type Amino Anhydride Monomers Macromolecules. 30: 764-769. DOI: 10.1021/Ma960982L |
0.308 |
|
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