| Year |
Citation |
Score |
| 2020 |
Sharma A, Saklani D, Thomas KRJ, Shahnawaz, Swayamprabha SS, Jou J. Synthesis and characterization of multi-substituted carbazole derivatives exhibiting aggregation-induced emission for OLED applications Organic Electronics. 86: 105864. DOI: 10.1016/J.Orgel.2020.105864 |
0.459 |
|
| 2020 |
Joseph V, Thomas KRJ, Sahoo S, Singh M, Jou J. Asymmetrically 2,7-difunctionalized carbazole-based donor-acceptor hybrids for deep blue electroluminescence applications Optical Materials. 108: 110159. DOI: 10.1016/J.Optmat.2020.110159 |
0.456 |
|
| 2020 |
Sharma A, Balasaravanan R, Thomas KRJ, Ram M, Dubey DK, Yadav RAK, Jou J. Tuning Photophysical and Electroluminescent Properties of Phenanthroimidazole Decorated Carbazoles with Donor and Acceptor Units: Beneficial Role of Cyano Substitution Dyes and Pigments. 108830. DOI: 10.1016/J.Dyepig.2020.108830 |
0.472 |
|
| 2019 |
Thomas KRJ, Venkateswararao A, Joseph V, Kumar S, Jou J. Polarity tuning of fluorene derivatives by chromophores to achieve efficient blue electroluminescent materials Organic Electronics. 64: 266-273. DOI: 10.1016/J.Orgel.2018.10.029 |
0.457 |
|
| 2019 |
Pathak A, Tomer T, Thomas KRJ, Fan M, Ho K. Fine tuning the absorption and photovoltaic properties of benzothiadiazole dyes by donor-acceptor interaction alternation via methyl position Electrochimica Acta. 304: 1-10. DOI: 10.1016/J.Electacta.2019.02.077 |
0.444 |
|
| 2019 |
Thomas KRJ, Venkateswararao A, Balasaravanan R, Li C, Ho K. Triazine-branched mono- and dianchoring organic dyes: Effect of acceptor arms on optical and photovoltaic properties Dyes and Pigments. 165: 182-192. DOI: 10.1016/J.Dyepig.2019.02.013 |
0.466 |
|
| 2019 |
Kumar S, Thomas KRJ, Li C, Fan M, Ho K. Effect of electron rich π-linkers on the functional properties of dyes featuring dithieno[3,2-b:2′,3′-d]pyrrole donor Dyes and Pigments. 160: 614-623. DOI: 10.1016/J.Dyepig.2018.08.035 |
0.479 |
|
| 2018 |
Joseph V, Thomas KRJ, Sahoo S, Singh M, Dubey DK, Jou JH. Vinyl-Linked Cyanocarbazole-Based Emitters: Effect of Conjugation and Terminal Chromophores on the Photophysical and Electroluminescent Properties. Acs Omega. 3: 16477-16488. PMID 31458283 DOI: 10.1021/acsomega.8b02198 |
0.383 |
|
| 2018 |
Konidena RK, Thomas KRJ, Pathak A, Dubey DK, Sahoo S, Jou JH. Tuning Photophysical and Electroluminescence Properties in Asymmetrically Tetrasubstituted Bipolar Carbazoles by Functional Group Disposition. Acs Applied Materials & Interfaces. PMID 29931980 DOI: 10.1021/Acsami.8B04566 |
0.433 |
|
| 2018 |
Sahoo S, Dubey DK, Singh M, Joseph V, Thomas KRJ, Jou J. Highly efficient deep-blue organic light emitting diode with a carbazole based fluorescent emitter Japanese Journal of Applied Physics. 57. DOI: 10.7567/Jjap.57.04Fl08 |
0.386 |
|
| 2018 |
Jou J, Li J, Sahoo S, Dubey DK, Yadav RAK, Joseph V, Thomas KRJ, Wang C, Jayakumar J, Cheng C. Enabling a 6.5% External Quantum Efficiency Deep-Blue Organic Light-Emitting Diode with a Solution-Processable Carbazole-Based Emitter Journal of Physical Chemistry C. 122: 24295-24303. DOI: 10.1021/Acs.Jpcc.8B07641 |
0.373 |
|
| 2018 |
Joseph V, Thomas KRJ, Sahoo S, Singh M, Jou J. Cyano-functionalized carbazole substituted pyrene derivatives for promising organic light-emitting diodes Dyes and Pigments. 158: 295-305. DOI: 10.1016/J.Dyepig.2018.05.038 |
0.438 |
|
| 2018 |
Joseph V, Thomas KRJ, Sahoo S, Singh M, Jou J. Simple carbazole based deep-blue emitters: The effect of spacer, linkage and end-capping cyano group on the photophysical and electroluminescent properties Dyes and Pigments. 151: 310-320. DOI: 10.1016/J.Dyepig.2017.12.061 |
0.461 |
|
| 2018 |
Saini A, Thomas KRJ, Huang Y, Ho K. Synthesis and characterization of naphthalimide-based dyes for dye sensitized solar cells Journal of Materials Science: Materials in Electronics. 29: 16565-16580. DOI: 10.1007/S10854-018-9750-4 |
0.459 |
|
| 2018 |
Thomas KRJ, Bodedla GB. T‐Shaped Benzimidazole Derivatives as Blue‐Emitting Materials: The Role of C2 Substituents on Photophysical Properties Asian Journal of Organic Chemistry. 7: 729-738. DOI: 10.1002/Ajoc.201800003 |
0.303 |
|
| 2017 |
Saini A, Thomas KRJ, Sachdev A, Gopinath P. Photophysics, Electrochemistry, Morphology, and Bioimaging Applications of New 1,8-Naphthalimide Derivatives Containing Different Chromophores. Chemistry, An Asian Journal. 12: 2612-2622. PMID 28783249 DOI: 10.1002/Asia.201700968 |
0.738 |
|
| 2017 |
Konidena RK, Thomas KRJ, Sahoo S, Dubey DK, Jou J. Multi-substituted deep-blue emitting carbazoles: a comparative study on photophysical and electroluminescence characteristics Journal of Materials Chemistry C. 5: 709-726. DOI: 10.1039/C6Tc04870F |
0.497 |
|
| 2017 |
Kumar S, Thomas KRJ, Li C, Ho K. Effect of electron-deficient linkers on the physical and photovoltaic properties of dithienopyrrole-based organic dyes Journal of Materials Science: Materials in Electronics. 28: 18404-18417. DOI: 10.1007/S10854-017-7787-4 |
0.463 |
|
| 2017 |
Joseph V, Thomas KRJ, Singh M, Sahoo S, Jou J. Manipulation of Donor–Acceptor Interactions in Carbazole‐Based Emitters by Chromophore Choice To Achieve Near‐UV Emission European Journal of Organic Chemistry. 2017: 6660-6670. DOI: 10.1002/Ejoc.201701285 |
0.449 |
|
| 2016 |
Konidena RK, Thomas KRJ, Singh M, Jou J. Thienylphenothiazine integrated pyrenes: an account on the influence of substitution patterns on their optical and electroluminescence properties Journal of Materials Chemistry C. 4: 4246-4258. DOI: 10.1039/C6Tc00354K |
0.45 |
|
| 2016 |
Saini A, Thomas KRJ. Bis-naphthalimides bridged by electron acceptors: optical and self-assembly characteristics Rsc Advances. 6: 71638-71651. DOI: 10.1039/C6Ra12776B |
0.406 |
|
| 2016 |
Karthik D, Thomas KRJ, Jou J, Chen Y. Synthesis, characterization and electroluminescence of carbazole-benzimidazole hybrids with thiophene/phenyl linker Dyes and Pigments. 133: 132-142. DOI: 10.1016/J.Dyepig.2016.05.046 |
0.471 |
|
| 2016 |
Saini A, Thomas KRJ, Li C, Ho K. Organic dyes containing fluorenylidene functionalized phenothiazine donors as sensitizers for dye sensitized solar cells Journal of Materials Science: Materials in Electronics. 27: 12392-12404. DOI: 10.1007/S10854-016-5146-5 |
0.47 |
|
| 2015 |
Konidena RK, Thomas KR, Kumar S, Wang YC, Li CJ, Jou JH. Phenothiazine decorated carbazoles: effect of substitution pattern on the optical and electroluminescent characteristics. The Journal of Organic Chemistry. 80: 5812-23. PMID 25951296 DOI: 10.1021/Acs.Joc.5B00787 |
0.427 |
|
| 2015 |
Bodedla GB, Thomas KRJ, Kumar S, Jou J, Li C. Phenothiazine-based bipolar green-emitters containing benzimidazole units: synthesis, photophysical and electroluminescence properties Rsc Advances. 5: 87416-87428. DOI: 10.1039/C5Ra18372C |
0.465 |
|
| 2015 |
Jou JH, Kumar S, Fang PH, Venkateswararao A, Thomas KRJ, Shyue JJ, Wang YC, Li TH, Yu HH. Highly efficient ultra-deep blue organic light-emitting diodes with a wet- and dry-process feasible cyanofluorene acetylene based emitter Journal of Materials Chemistry C. 3: 2182-2194. DOI: 10.1039/C4Tc02547D |
0.385 |
|
| 2015 |
Venkateswararao A, Thomas KRJ, Li C, Ho K. Functional tuning of organic dyes containing 2,7-carbazole and other electron-rich segments in the conjugation pathway Rsc Advances. 5: 17953-17966. DOI: 10.1039/C4Ra15234D |
0.491 |
|
| 2015 |
Karthik D, Thomas KRJ, Jou JH, Kumar S, Chen YL, Jou YC. Deep-blue emitting pyrene-benzimidazole conjugates for solution processed organic light-emitting diodes Rsc Advances. 5: 8727-8738. DOI: 10.1039/C4Ra11043A |
0.442 |
|
| 2015 |
Bolisetty MNKP, Li C, Thomas KRJ, Bodedla GB, Ho K. Benzothiadiazole-based organic dyes with pyridine anchors for dye-sensitized solar cells: effect of donor on optical properties Tetrahedron. 71: 4203-4212. DOI: 10.1016/J.Tet.2015.04.089 |
0.495 |
|
| 2015 |
Baheti A, Gajjela SR, Balaya P, Thomas KRJ. Synthesis, optical, electrochemical and photovoltaic properties of organic dyes containing trifluorenylamine donors Dyes and Pigments. 113: 78-86. DOI: 10.1016/J.Dyepig.2014.07.036 |
0.468 |
|
| 2015 |
Venkateswararao A, Thomas KRJ, Lee C, Ho K. Effect of Auxiliary Chromophores on the Optical, Electrochemical, and Photovoltaic Properties of Carbazole‐Based Dyes Asian Journal of Organic Chemistry. 4: 69-80. DOI: 10.1002/Ajoc.201402235 |
0.471 |
|
| 2015 |
Kumar D, Thomas KRJ, Lee C, Ho K. Triarylamine-Free Pyrenoimidazole-Containing Organic Dyes with Different π-Linkers for Dye-Sensitized Solar Cells Asian Journal of Organic Chemistry. 4: 164-172. DOI: 10.1002/Ajoc.201402214 |
0.475 |
|
| 2014 |
Kumar D, Thomas KR, Lee CP, Ho KC. Organic dyes containing fluorene decorated with imidazole units for dye-sensitized solar cells. The Journal of Organic Chemistry. 79: 3159-72. PMID 24628443 DOI: 10.1021/Jo500330R |
0.476 |
|
| 2014 |
Venkateswararao A, Thomas KR, Lee CP, Li CT, Ho KC. Organic dyes containing carbazole as donor and π-linker: optical, electrochemical, and photovoltaic properties. Acs Applied Materials & Interfaces. 6: 2528-39. PMID 24456063 DOI: 10.1021/Am404948W |
0.483 |
|
| 2014 |
Bodedla GB, Thomas KRJ, Li C, Ho K. Functional tuning of phenothiazine-based dyes by a benzimidazole auxiliary chromophore: an account of optical and photovoltaic studies Rsc Advances. 4: 53588-53601. DOI: 10.1039/C4Ra09300C |
0.468 |
|
| 2014 |
Konidena RK, Thomas KRJ. Selective naked-eye cyanide detection in aqueous media using a carbazole-derived fluorescent dye Rsc Advances. 4: 22902-22910. DOI: 10.1039/C4Ra02636E |
0.376 |
|
| 2014 |
Baheti A, Thomas KRJ, Lee C, Li C, Ho K. Organic dyes containing fluoren-9-ylidene chromophores for efficient dye-sensitized solar cells Journal of Materials Chemistry. 2: 5766-5779. DOI: 10.1039/C3Ta15456D |
0.47 |
|
| 2014 |
Kumar S, Karthik D, Thomas KJ, Hundal MS. Synthesis and characterization of polybrominated fluorenes and their conversion to polyphenylated fluorenes and cyclopenta[def]triphenylene Tetrahedron Letters. 55: 1931-1935. DOI: 10.1016/J.Tetlet.2014.02.002 |
0.329 |
|
| 2014 |
Lin L, Yeh M, Lee C, Chang J, Baheti A, Vittal R, Thomas KRJ, Ho K. Insights into the co-sensitizer adsorption kinetics for complementary organic dye-sensitized solar cells Journal of Power Sources. 247: 906-914. DOI: 10.1016/J.Jpowsour.2013.08.127 |
0.372 |
|
| 2014 |
Baheti A, Thomas KRJ, Lin L, Lee K. Monoanchoring (D‐D‐π‐A) and Dianchoring (D‐D‐(π‐A)2) Organic Dyes Featuring Triarylamine Donors Composed of Fluorene and Carbazole Asian Journal of Organic Chemistry. 3: 886-898. DOI: 10.1002/Ajoc.201402073 |
0.391 |
|
| 2013 |
Kumar D, Thomas KR, Lin CC, Jou JH. Pyrenoimidazole-based deep-blue-emitting materials: optical, electrochemical, and electroluminescent characteristics. Chemistry, An Asian Journal. 8: 2111-24. PMID 23740829 DOI: 10.1002/Asia.201300271 |
0.477 |
|
| 2013 |
Thomas KRJ, Baheti A. Fluorene based organic dyes for dye sensitised solar cells: structure–property relationships Materials Technology. 28: 71-87. DOI: 10.1179/1753555712Y.0000000036 |
0.426 |
|
| 2013 |
Venkateswararao A, Thomas KRJ, Lee C, Ho K. Synthesis and characterization of organic dyes containing 2,7-disubstituted carbazole π-linker Tetrahedron Letters. 54: 3985-3989. DOI: 10.1016/J.Tetlet.2013.05.069 |
0.449 |
|
| 2013 |
Kumar D, Thomas KRJ, Chen Y, Jou Y, Jou J. Synthesis, optical properties, and blue electroluminescence of fluorene derivatives containing multiple imidazoles bearing polyaromatic hydrocarbons Tetrahedron. 69: 2594-2602. DOI: 10.1016/J.Tet.2013.01.046 |
0.453 |
|
| 2013 |
Baheti A, Thomas KRJ, Lee C, Ho K. Synthesis and characterization of dianchoring organic dyes containing 2,7-diaminofluorene donors as efficient sensitizers for dye-sensitized solar cells Organic Electronics. 14: 3267-3276. DOI: 10.1016/J.Orgel.2013.09.038 |
0.464 |
|
| 2013 |
Chang J, Lee C, Kumar D, Chen P, Lin L, Thomas KRJ, Ho K. Co-sensitization promoted light harvesting for organic dye-sensitized solar cells using unsymmetrical squaraine dye and novel pyrenoimidazole-based dye Journal of Power Sources. 240: 779-785. DOI: 10.1016/J.Jpowsour.2013.04.075 |
0.399 |
|
| 2012 |
Baheti A, Thomas KR, Lee CP, Ho KC. Fine tuning the performance of DSSCs by variation of the π-spacers in organic dyes that contain a 2,7-diaminofluorene donor. Chemistry, An Asian Journal. 7: 2942-54. PMID 23023960 DOI: 10.1002/Asia.201200752 |
0.487 |
|
| 2012 |
Thomas KR, Kapoor N, Bolisetty MN, Jou JH, Chen YL, Jou YC. Pyrene-fluorene hybrids containing acetylene linkage as color-tunable emitting materials for organic light-emitting diodes. The Journal of Organic Chemistry. 77: 3921-32. PMID 22443338 DOI: 10.1021/Jo300285V |
0.468 |
|
| 2012 |
Thomas KR, Kapoor N, Lee CP, Ho KC. Organic dyes containing pyrenylamine-based cascade donor systems with different aromatic π linkers for dye-sensitized solar cells: optical, electrochemical, and device characteristics. Chemistry, An Asian Journal. 7: 738-50. PMID 22298333 DOI: 10.1002/Asia.201100849 |
0.474 |
|
| 2012 |
Sharma GD, Mikroyannidis JA, Roy MS, Thomas KRJ, Ball RJ, Kurchania R. Dithienylthienothiadiazole-based organic dye containing two cyanoacrylic acid anchoring units for dye-sensitized solar cells Rsc Advances. 2: 11457-11464. DOI: 10.1039/C2Ra21718J |
0.41 |
|
| 2012 |
Sharma GD, Mikroyannidis JA, Kurchania R, Thomas KRJ. Organic bulk heterojunction solar cells based on solution processable small molecules (A-π-A) featuring 2-(4-nitrophenyl) acrylonitrile acceptors and phthalimide-based π-linkers Journal of Materials Chemistry. 22: 13986-13995. DOI: 10.1039/C2Jm16915K |
0.445 |
|
| 2012 |
Singh SP, Roy MS, Thomas KRJ, Balaiah S, Bhanuprakash K, Sharma GD. New triphenylamine-based organic dyes with different numbers of anchoring groups for dye-sensitized solar cells Journal of Physical Chemistry C. 116: 5941-5950. DOI: 10.1021/Jp210971U |
0.449 |
|
| 2012 |
Thomas KRJ, Kapoor N, Roy MS, Sharma GD. Retraction notice to: Efficient bulk heterojunction solar cells using tetrasubstituted pyrene derivatives as donors [Org. Electron. 13 (2012) 2201–2209] Organic Electronics. 13. DOI: 10.1016/J.Orgel.2012.08.011 |
0.377 |
|
| 2012 |
Sharma GD, Mikroyannidis JA, Sharma SS, Roy MS, Thomas KRJ. Corrigendum to “Efficient bulk heterojunction photovoltaic devices based on diketopyrrolopyrrole containing small molecule as donor and modified PCBM derivatives as electron acceptors” [Organic Electronics 13 (2012) 652–666] Organic Electronics. 13: 1763-1764. DOI: 10.1016/J.Orgel.2012.05.006 |
0.358 |
|
| 2012 |
Lin LY, Lee CP, Yeh MH, Baheti A, Vittal R, Thomas KRJ, Ho KC. A novel 2,7-diaminofluorene-based organic dye for a dye-sensitized solar cell Journal of Power Sources. 215: 122-129. DOI: 10.1016/J.Jpowsour.2012.04.084 |
0.424 |
|
| 2012 |
Singh P, Baheti A, Thomas KRJ, Lee C, Ho K. Fluorene-based organic dyes containing acetylene linkage for dye-sensitized solar cells Dyes and Pigments. 95: 523-533. DOI: 10.1016/J.Dyepig.2012.06.004 |
0.463 |
|
| 2011 |
Baheti A, Lee CP, Thomas KR, Ho KC. Pyrene-based organic dyes with thiophene containing π-linkers for dye-sensitized solar cells: optical, electrochemical and theoretical investigations. Physical Chemistry Chemical Physics : Pccp. 13: 17210-21. PMID 21879061 DOI: 10.1039/C1Cp21714C |
0.492 |
|
| 2011 |
Singh P, Baheti A, Thomas KR. Synthesis and optical properties of acidochromic amine-substituted benzo[a]phenazines. The Journal of Organic Chemistry. 76: 6134-45. PMID 21644579 DOI: 10.1021/Jo200857P |
0.437 |
|
| 2011 |
Baheti A, Singh P, Lee CP, Thomas KR, Ho KC. 2,7-Diaminofluorene-based organic dyes for dye-sensitized solar cells: effect of auxiliary donor on optical and electrochemical properties. The Journal of Organic Chemistry. 76: 4910-20. PMID 21557605 DOI: 10.1021/Jo200501B |
0.482 |
|
| 2011 |
Tyagi P, Venkateswararao A, Thomas KR. Solution processable indoloquinoxaline derivatives containing bulky polyaromatic hydrocarbons: synthesis, optical spectra, and electroluminescence. The Journal of Organic Chemistry. 76: 4571-81. PMID 21539382 DOI: 10.1021/Jo2004764 |
0.438 |
|
| 2011 |
Kumar D, Thomas KR, Lee CP, Ho KC. Novel pyrenoimidazole-based organic dyes for dye-sensitized solar cells. Organic Letters. 13: 2622-5. PMID 21506594 DOI: 10.1021/Ol2006874 |
0.45 |
|
| 2011 |
Lee K, Hsu Y, Ikegami M, Miyasaka T, Thomas KRJ, Lin JT, Ho K. Co-sensitization promoted light harvesting for plastic dye-sensitized solar cells Journal of Power Sources. 196: 2416-2421. DOI: 10.1016/J.Jpowsour.2010.10.041 |
0.371 |
|
| 2011 |
Kumar D, Thomas KRJ. Optical properties of pyrene and anthracene containing imidazoles: Experimental and theoretical investigations Journal of Photochemistry and Photobiology a-Chemistry. 218: 162-173. DOI: 10.1016/J.Jphotochem.2010.12.018 |
0.427 |
|
| 2011 |
Thomas KRJ, Singh P, Baheti A, Hsu Y, Ho K, Lin JT. Electro-optical properties of new anthracene based organic dyes for dye-sensitized solar cells Dyes and Pigments. 91: 33-43. DOI: 10.1016/J.Dyepig.2011.02.006 |
0.455 |
|
| 2011 |
Baheti A, Singh P, Thomas KRJ. The synthesis and spectral characterization of red dyes containing biphenyl or fluorene conjugation and dicyanovinyl acceptors Dyes and Pigments. 88: 195-203. DOI: 10.1016/J.Dyepig.2010.06.008 |
0.432 |
|
| 2010 |
Thomas KR, Tyagi P. Synthesis, spectra, and theoretical investigations of the triarylamines based on 6H-indolo[2,3-b]quinoxaline. The Journal of Organic Chemistry. 75: 8100-11. PMID 21053895 DOI: 10.1021/Jo1016663 |
0.4 |
|
| 2010 |
Chen CH, Hsu YC, Chou HH, Thomas KR, Lin JT, Hsu CP. Dipolar compounds containing fluorene and a heteroaromatic ring as the conjugating bridge for high-performance dye-sensitized solar cells. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3184-93. PMID 20119994 DOI: 10.1002/Chem.200903151 |
0.461 |
|
| 2010 |
Kapoor N, Thomas KRJ. Fluoranthene-based triarylamines as hole-transporting and emitting materials for efficient electroluminescent devices New Journal of Chemistry. 34: 2739-2748. DOI: 10.1039/C0Nj00415D |
0.458 |
|
| 2009 |
Baheti A, Tyagi P, Thomas KRJ, Hsu Y, Lin JT. Simple Triarylamine-Based Dyes Containing Fluorene and Biphenyl Linkers for Efficient Dye-Sensitized Solar Cells Journal of Physical Chemistry C. 113: 8541-8547. DOI: 10.1021/Jp902206G |
0.453 |
|
| 2009 |
Lee K, Suryanarayanan V, Huang J, Thomas KRJ, Lin JT, Ho K. Enhancing the performance of dye-sensitized solar cells based on an organic dye by incorporating TiO2 nanotube in a TiO2 nanoparticle film Electrochimica Acta. 54: 4123-4130. DOI: 10.1016/J.Electacta.2009.02.052 |
0.404 |
|
| 2008 |
Thomas KR, Huang TH, Lin JT, Pu SC, Cheng YM, Hsieh CC, Tai CP. Donor-acceptor interactions in red-emitting thienylbenzene-branched dendrimers with benzothiadiazole core. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 11231-41. PMID 18991307 DOI: 10.1002/Chem.200801694 |
0.401 |
|
| 2008 |
Hsu C, Lee K, Huang J, Thomas KRJ, Lin JT, Ho K. A novel photoelectrochromic device with dual application based on poly(3,4-alkylenedioxythiophene) thin film and an organic dye Journal of Power Sources. 185: 1505-1508. DOI: 10.1016/J.Jpowsour.2008.09.031 |
0.339 |
|
| 2007 |
Velusamy M, Thomas KR, Chen CH, Lin JT, Wen YS, Hsieh WT, Lai CH, Chou PT. Synthesis, structure and electroluminescent properties of cyclometalated iridium complexes possessing sterically hindered ligands. Dalton Transactions (Cambridge, England : 2003). 3025-34. PMID 17622420 DOI: 10.1039/B618311E |
0.394 |
|
| 2007 |
Lee K, Suryanarayanan V, Ho K, Thomas KRJ, Lin JT. Effects of co-adsorbate and additive on the performance of dye-sensitized solar cells: A photophysical study Solar Energy Materials and Solar Cells. 91: 1426-1431. DOI: 10.1016/J.Solmat.2007.03.009 |
0.394 |
|
| 2006 |
Thomas KRJ, Lin JT, Tsai C, Lin H. Star-like fluorene based polyamines: non-conjugated building blocks for light-harvesting materials Tetrahedron. 62: 3517-3522. DOI: 10.1016/J.Tet.2006.02.001 |
0.429 |
|
| 2006 |
Lin H, Tsai C, Lin J, Thomas KRJ. Novel red and white PLED devices consisting of PVK blended with blue-emitting fluorene derivatives and carbazole dopants Synthetic Metals. 156: 1155-1160. DOI: 10.1016/J.Synthmet.2006.05.015 |
0.351 |
|
| 2005 |
Lee S, Thomas KR, Thayumanavan S, Bardeen CJ. Dependence of the two-photon absorption cross section on the conjugation of the phenylacetylene linker in dipolar donor-bridge-acceptor chromophores. The Journal of Physical Chemistry. A. 109: 9767-74. PMID 16833290 DOI: 10.1021/Jp053864L |
0.374 |
|
| 2005 |
Thomas KR, Lin JT, Hsu YC, Ho KC. Organic dyes containing thienylfluorene conjugation for solar cells. Chemical Communications (Cambridge, England). 4098-100. PMID 16091812 DOI: 10.1039/B506732D |
0.409 |
|
| 2005 |
Thomas KR, Velusamy M, Lin JT, Chien CH, Tao YT, Wen YS, Hu YH, Chou PT. Efficient red-emitting cyclometalated Iridium(III) complexes containing lepidine-based ligands. Inorganic Chemistry. 44: 5677-85. PMID 16060618 DOI: 10.1021/Ic050385S |
0.387 |
|
| 2005 |
Thomas KRJ, Velusamy M, Lin JT, Chuen CH, Tao Y. Hexaphenylphenylene dendronised pyrenylamines for efficient organic light-emitting diodes Journal of Materials Chemistry. 15: 4453-4459. DOI: 10.1039/B509325B |
0.371 |
|
| 2005 |
Thomas KRJ, Velusamy M, Lin JT, Chuen †aC, Tao †Y. Chromophore-labeled quinoxaline derivatives as efficient electroluminescent materials Chemistry of Materials. 17: 1860-1866. DOI: 10.1021/Cm047705A |
0.426 |
|
| 2005 |
Velusamy M, Thomas KRJ, Lin JT, Wen YS. Benzo[1,2,5]selenadiazole bridged amines : electro-optical properties Tetrahedron Letters. 46: 7647-7651. DOI: 10.1016/J.Tetlet.2005.08.166 |
0.4 |
|
| 2004 |
Thomas KR, Velusamy M, Lin JT, Sun SS, Tao YT, Chuen CH. Energy harvesting star-shaped molecules for electroluminescence applications. Chemical Communications (Cambridge, England). 2328-9. PMID 15490004 DOI: 10.1039/B409800E |
0.327 |
|
| 2004 |
Thomas KRJ, Lin JT, and YT,, Chuen† C. New carbazole-oxadiazole dyads for electroluminescent devices: Influence of acceptor substituents on luminescent and thermal properties Chemistry of Materials. 16: 5437-5444. DOI: 10.1021/Cm048794U |
0.398 |
|
| 2004 |
Thomas KRJ, Velusamy M, Lin JT, Tao Y‐, Chuen C‐. Cyanocarbazole Derivatives for High-Performance Electroluminescent Devices † Advanced Functional Materials. 14: 387-392. DOI: 10.1002/Adfm.200305144 |
0.343 |
|
| 2004 |
Thomas KRJ, Lin JT, Velusamy M, Tao YT, Chuen CH. Color Tuning in Benzo[1,2,5]thiadiazole‐Based Small Molecules by Amino Conjugation/Deconjugation: Bright Red‐Light‐Emitting Diodes Advanced Functional Materials. 14: 83-90. DOI: 10.1002/Adfm.200304486 |
0.415 |
|
| 2003 |
Kundu P, Thomas KRJ, Lin JT, Tao Y-, Chien C-. High‐Tg Carbazole Derivatives as Blue‐Emitting Hole‐Transporting Materials for Electroluminescent Devices Advanced Functional Materials. 13: 445-452. DOI: 10.1002/Adfm.200304308 |
0.381 |
|
| 2002 |
Thomas KRJ, Lin JT, Tao Y, Chuen CH. Electroluminescent bipolar compounds containing quinoxaline or pyridopyrazine and triarylamine segments Journal of Materials Chemistry. 12: 3516-3522. DOI: 10.1039/B206126K |
0.4 |
|
| 2002 |
Thomas KRJ, Lin JT, and YT,, Chuen† C. Green and Yellow Electroluminescent Dipolar Carbazole Derivatives: Features and Benefits of Electron-Withdrawing Segments Chemistry of Materials. 14: 3852-3859. DOI: 10.1021/Cm0202512 |
0.403 |
|
| 2002 |
Thomas KRJ, Lin JT, Tao Y, Chuen C. Quinoxalines incorporating triarylamines: Potential electroluminescent materials with tunable emission characteristics Chemistry of Materials. 14: 2796-2802. DOI: 10.1021/Cm0201100 |
0.404 |
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| 2002 |
Thomas KRJ, Lin JT, Tao Y, Ko C. New Star-shaped Luminescent Triarylamines: Synthesis, Thermal, Photophysical and Electroluminescent Characteristics Chemistry of Materials. 14: 1354-1361. DOI: 10.1021/Cm010976Q |
0.389 |
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| 2002 |
Ko C, ,† YT, Lin aJT, Thomas KRJ. Light-Emitting Diodes Based on a Carbazole-Derivatized Dopant: Origin of Dopant Excitation as a Function of the Device Structure Chemistry of Materials. 14: 357-361. DOI: 10.1021/Cm0106365 |
0.371 |
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| 2002 |
Thomas KRJ, Lin JT, Chang C, Chuen C, Cheng C. Zinc(II) and Ruthenium(II) Complexes of Novel Fluorene Substituted Terpyridine Ligands: Synthesis, Spectroscopy and Electrochemistry Journal of the Chinese Chemical Society. 49: 833-840. DOI: 10.1002/Jccs.200200119 |
0.364 |
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| 2001 |
Thomas KR, Lin JT, Tao YT, Ko CW. Light-emitting carbazole derivatives: potential electroluminescent materials. Journal of the American Chemical Society. 123: 9404-11. PMID 11562223 DOI: 10.1021/Ja010819S |
0.404 |
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| 2001 |
Manikandan P, Muthukumaran R, Thomas KR, Varghese B, Chandramouli GV, Manoharan PT. Copper(II) azide complexes of aliphatic and aromatic amine based tridentate ligands: novel structure, spectroscopy, and magnetic properties. Inorganic Chemistry. 40: 2378-89. PMID 11327916 DOI: 10.1021/Ic0009223 |
0.36 |
|
| 2001 |
Thomas KRJ, Lin JT, Lin Y, Tsai C, Sun S. Self-Assembly Molecular Architectures Incorporating Fluorene- and Carbazole-Based Bichromic Oligopyridines. Novel Photoactive Materials Organometallics. 20: 2262-2269. DOI: 10.1021/Om010035N |
0.375 |
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| 2001 |
Thomas KRJ, Lin JT, Lin †H, Chang ‡aC, Chuen‡ C. Ruthenium and Rhenium Complexes of Fluorene-Based Bipyridine Ligands: Synthesis, Spectra, and Electrochemistry Organometallics. 20: 557-563. DOI: 10.1021/Om000764N |
0.397 |
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| 2001 |
Thomas KRJ, Lin JT. Star-shaped polyferrocenes based on thiophene and triphenylamine: synthesis, spectroscopy and electrochemistry Journal of Organometallic Chemistry. 637: 139-144. DOI: 10.1016/S0022-328X(01)00885-3 |
0.355 |
|
| 2000 |
Manikandan P, Thomas KRJ, Manoharan PT. Structural and spectral diversities in copper(II) complexes of 2,6-bis(3,5-dimethylpyrazol-1-ylmethyl)pyridine Journal of the Chemical Society-Dalton Transactions. 2779-2785. DOI: 10.1039/B002289F |
0.394 |
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| 2000 |
Karunakaran C, Thomas KRJ, Shunmugasundarama A, Murugesan R. Crystal structure and spectroscopy of a hydrogen-bridged one-dimensional Cu(II) complex containing both octahedral and square pyramidal geometries in the same unit cell Journal of Chemical Crystallography. 30: 351-357. DOI: 10.1023/A:1009569426357 |
0.334 |
|
| 2000 |
Karunakaran C, Thomas KRJ, Asurname A, Murugesan R. Synthesis, Structure and Spectroscopy of Clathrate Inclusion Compounds of Cobalt(II), Cadmium(II) and Zinc(II) trans-4-styrylpyridine nitrates as Host with trans-4-styrylpyridine as Guest (2 : 1) Journal of Inclusion Phenomena and Macrocyclic Chemistry. 38: 233-249. DOI: 10.1023/A:1008137311908 |
0.344 |
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| 1999 |
Karunakaran C, Thomas KRJ, Shunmugasundaram A, Murugesan R. X-ray crystal structure and spectroscopy of a pseudo-square pyramidal Cu(II) complex, trans-dinitratotetrakis (trans-4-styrylpyridine)copper(II) Journal of Chemical Crystallography. 29: 413-420. DOI: 10.1023/A:1009510910121 |
0.363 |
|
| 1999 |
Thomas KRJ, Lin aJT, Lin K. Ferrocene End-Capped Palladium(Ii) And Platinum(Ii) Complexes With Thiophene Spacers Organometallics. 18: 5285-5291. DOI: 10.1021/Om990556Z |
0.329 |
|
| 1999 |
Thomas KRJ, Lin JT, Wen YS. Synthesis, spectroscopy and structure of new push–pull ferrocene complexes containing heteroaromatic rings (thiophene and furan) in the conjugation chain Journal of Organometallic Chemistry. 575: 301-309. DOI: 10.1016/S0022-328X(98)01009-2 |
0.384 |
|
| 1998 |
Velusamy M, Palaniandavar M, Thomas KRJ. Cis-facial coordination of bis(pyrid-2-ylmethyl)amine (bpma). Synthesis, structure and spectral behaviour of [Ni(bpma)2]2+ Polyhedron. 17: 2179-2186. DOI: 10.1016/S0277-5387(98)00059-X |
0.326 |
|
| 1995 |
Thomas KRJ, Chandrasekhar V, Bryan CD, Cordes AW. HETEROBIMETALLIC (PD,PT,CU) COMPLEXES OF HEXAPYRAZOLYLCYCLOTRIPHOSPHAZENEVIASIMULTANEOUS GEMINAL (N2) AND NONGEMINAL (N3) COORDINATION MODES Journal of Coordination Chemistry. 35: 337-348. DOI: 10.1080/00958979508024046 |
0.507 |
|
| 1995 |
Thomas K, Tharmaraj P, Chandrasekhar V, Scott SR, Wallace Cordes A. Five-coordinate copper(II) complexes of GEM-N3P3Ph2(dmpz)4 Polyhedron. 14: 977-982. DOI: 10.1016/0277-5387(94)00363-J |
0.509 |
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| 1994 |
Cordes AW, Folkert S, Bryan CD, Chandrasekhar V, Thomas KRJ. 2,2,4,4-Tetrakis(3,5-dimethylpyrazol-1-yl)-2λ5,4λ5,6λ5-cyclotriphosphaza-1,3,5-triene-6-spiro-2'-1',3'-diaza-2'-phosphacyclohexane, C23H36N13P3 Acta Crystallographica Section C Crystal Structure Communications. 50: 1976-1978. DOI: 10.1107/S0108270194007006 |
0.386 |
|
| 1994 |
Thomas KRJ, Tharmaraj P, Chandrasekhar V, Tiekink ERT. Synthesis and characterization of mononuclear nickel(II) and cobalt(II) complexes of 2,2,4,4-tetrakis(3,5-dimethylpyrazolyl)-6,6-diphenyl-2λ5,4λ5,6λ5-cyclotriphosphaza-1,3,5-triene L: crystal structure of [NiLCl2] Journal of the Chemical Society-Dalton Transactions. 1301-1304. DOI: 10.1039/Dt9940001301 |
0.438 |
|
| 1994 |
Thomas KRJ, Tharmaraj P, Chandrasekhar V, Bryan CD, Cordes AW. Synthesis, Spectroscopy, and Electrochemistry of Ternary Copper(II) Complexes with 2,2-Diphenyl-4,4,6,6-tetrakis(3,5-dimethylpyrazolyl)cyclotriphosphazene and Nitrogenous Bases. X-ray Structures of N3P3Ph2(3,5-Me2Pz)4.cntdot.Cu(ClO4)2.cntdot.2H2O and N3P3Ph2(3,5-Me2Pz)4.cntdot.Cu(ClO4)2.cntdot.2ImH Inorganic Chemistry. 33: 5382-5390. DOI: 10.1021/Ic00102A008 |
0.483 |
|
| 1993 |
Thomas KRJ, Chandrasekhar V, Scott SR, Hallford R, Cordes AW. Synthesis and spectroscopy of mono- and di-nuclear copper complexes of a pyrazolylcyclotriphosphazene. Crystal structure of an unusual cyclotriphosphazene-bridged dicopper complex Journal of the Chemical Society-Dalton Transactions. 2589-2594. DOI: 10.1039/Dt9930002589 |
0.524 |
|
| 1993 |
Thomas KRJ, Chandrasekhar V, Pal P, Scott SR, Hallford R, Cordes AW. Unusual tridentate N3 capping coordination behavior of hexakis(3,5-dimethylpyrazolyl)cyclotriphosphazene, N3P3(3,5-Me2Pz)6: synthesis, spectroscopy, and electrochemistry of mono- and dinuclear copper(II) complexes and the x-ray structure of N3P3(3,5-Me2Pz)6.cntdot.CuCl2 Inorganic Chemistry. 32: 606-611. DOI: 10.1021/Ic00057A020 |
0.434 |
|
| 1993 |
Chandrasekhar V, Thomas KRJ. Coordination and organometallic chemistry of cyclophosphazenes and polyphosphazenes Applied Organometallic Chemistry. 7: 1-31. DOI: 10.1002/Aoc.590070102 |
0.467 |
|
| 1992 |
Chandrasekhar V, Muralidhara MG, Thomas KRJ, Tiekink ERT. Isolation and x-ray crystal structure of (phenylselenito)triphenyltin: the first example of an organotin ester of phenylseleninic acid Inorganic Chemistry. 31: 4707-4708. DOI: 10.1021/Ic00048A048 |
0.446 |
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