Year |
Citation |
Score |
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 |
0.675 |
|
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 |
0.685 |
|
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 |
0.317 |
|
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 |
0.696 |
|
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 |
0.691 |
|
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 |
0.68 |
|
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 |
0.699 |
|
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 |
0.708 |
|
2013 |
Chang YL, Kamino BA, Wang Z, Helander MG, Rao Y, Chai L, Wang S, Bender TP, Lu ZH. Highly efficient greenish-yellow phosphorescent organic light-emitting diodes based on interzone exciton transfer Advanced Functional Materials. 23: 3204-3211. DOI: 10.1002/Adfm.201202944 |
0.674 |
|
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 |
0.695 |
|
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 |
0.695 |
|
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 |
0.721 |
|
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 |
0.672 |
|
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 |
0.676 |
|
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 |
0.695 |
|
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 |
0.682 |
|
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 |
0.702 |
|
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