{"id":12200,"date":"2016-05-11T15:09:11","date_gmt":"2016-05-11T06:09:11","guid":{"rendered":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/?page_id=12200"},"modified":"2022-12-09T21:07:31","modified_gmt":"2022-12-09T12:07:31","slug":"%e5%84%98%e7%94%b0%e3%80%80%e6%ad%a3%e5%8f%b2","status":"publish","type":"page","link":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/staff-2\/%e5%84%98%e7%94%b0%e3%80%80%e6%ad%a3%e5%8f%b2\/","title":{"rendered":"\u5118\u7530\u3000\u6b63\u53f2"},"content":{"rendered":"
\"\"<\/div>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
\u7565\u6b74<\/th>\n<\/tr>\n
2003.3<\/td>\n\u56fd\u7acb\u7fa4\u99ac\u5de5\u696d\u9ad8\u7b49\u5c02\u9580\u5b66\u6821 \u7269\u8cea\u5de5\u5b66\u79d1 \u5352\u696d<\/td>\n<\/tr>\n
2005.3<\/td>\n\u56fd\u7acb\u7fa4\u99ac\u5de5\u696d\u9ad8\u7b49\u5c02\u9580\u5b66\u6821\u5c02\u653b\u79d1 \u74b0\u5883\u5de5\u5b66\u5c02\u653b \u4fee\u4e86<\/td>\n<\/tr>\n
2007.3<\/td>\n\u6771\u4eac\u5de5\u696d\u5927\u5b66\u5927\u5b66\u9662 \u7dcf\u5408\u7406\u5de5\u5b66\u7814\u7a76\u79d1 \u535a\u58eb\u524d\u671f\u8ab2\u7a0b\u3000\u7269\u8cea\u96fb\u5b50\u5316\u5b66\u5c02\u653b \u4fee\u4e86<\/td>\n<\/tr>\n
2010.3<\/td>\n\u6771\u4eac\u5de5\u696d\u5927\u5b66\u5927\u5b66\u9662 \u7dcf\u5408\u7406\u5de5\u5b66\u7814\u7a76\u79d1 \u535a\u58eb\u5f8c\u671f\u8ab2\u7a0b\u3000\u7269\u8cea\u96fb\u5b50\u5316\u5b66\u5c02\u653b \u4fee\u4e86<\/td>\n<\/tr>\n
2009.4-2010.3<\/td>\n\u65e5\u672c\u5b66\u8853\u632f\u8208\u4f1a \u7279\u5225\u7814\u7a76\u54e1<\/td>\n<\/tr>\n
2009.9-2010.12<\/td>\nUniversity of Washington \u8a2a\u554f\u7814\u7a76\u54e1<\/td>\n<\/tr>\n
2010.4-2011.9<\/td>\nBowling Green State University(\u30dc\u30fc\u30ea\u30f3\u30b0\u30b0\u30ea\u30fc\u30f3\u5dde\u7acb\u5927\u5b66) \u535a\u58eb\u7814\u7a76\u54e1<\/td>\n<\/tr>\n
2015.8\u20132015.12<\/td>\nJohannes Kepler Universitat\u8a2a\u554f\u7814\u7a76\u54e1<\/td>\n<\/tr>\n
2011.10\u20132016.1<\/td>\n\u5c71\u5f62\u5927\u5b66\u5927\u5b66\u9662\u7406\u5de5\u5b66\u7814\u7a76\u79d1 \u52a9\u6559<\/td>\n<\/tr>\n
2016.2\u20132018.6<\/td>\n\u4e5d\u5dde\u5927\u5b66\u6700\u5148\u7aef\u6709\u6a5f\u5149\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u7814\u7a76\u30bb\u30f3\u30bf\u30fc \u52a9\u6559<\/td>\n<\/tr>\n
2018.6\u20132019-3<\/td>\n\u4e5d\u5dde\u5927\u5b66\u5206\u5b50\u30b7\u30b9\u30c6\u30e0\u30c7\u30d0\u30a4\u30b9\u56fd\u969b\u30ea\u30fc\u30c0\u30fc\u6559\u80b2\u30bb\u30f3\u30bf\u30fc \u52a9\u6559<\/td>\n<\/tr>\n
2019.4\u2013\u73fe\u5728<\/td>\n\u4e5d\u5dde\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u9662\u5fdc\u7528\u5316\u5b66\u90e8\u9580 \u52a9\u6559<\/td>\n<\/tr>\n
\u5b66\u4f4d<\/th>\n<\/tr>\n
\u535a\u58eb\uff08\u7406\u5b66\uff09<\/td>\n<\/tr>\n
\u6240\u5c5e\u5b66\u4f1a<\/th>\n<\/tr>\n
\u65e5\u672c\u5316\u5b66\u4f1a\u3001\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u3001\u5fdc\u7528\u7269\u7406\u5b66\u4f1a\u3001\u6709\u6a5fEL\u8a0e\u8ad6\u4f1a<\/td>\n<\/tr>\n
\u7814\u7a76\u5206\u91ce<\/th>\n<\/tr>\n
\u69cb\u9020\u6709\u6a5f\u5316\u5b66\u3001\u6709\u6a5f\u5408\u6210\u5316\u5b66\u3001\u6709\u6a5f\u96fb\u5b50\u30c7\u30d0\u30a4\u30b9<\/td>\n<\/tr>\n
\u53d7\u8cde\u6b74<\/th>\n<\/tr>\n
\u4ee4\u548c4\u5e74\u5ea6\u79d1\u5b66\u6280\u8853\u5206\u91ce\u306e\u6587\u90e8\u79d1\u5b66\u5927\u81e3\u8868\u5f70 \u82e5\u624b\u79d1\u5b66\u8005\u8cde<\/td>\n<\/tr>\n
\u6709\u6a5fEL\u8a0e\u8ad6\u4f1a \u8b1b\u6f14\u5968\u52b1\u8cde\u53d7\u8cde\u3001\u4ed6<\/td>\n<\/tr>\n
\u8da3\u5473<\/th>\n<\/tr>\n
\u6599\u7406\u3001\u304a\u9152\u3001\u30dc\u30fc\u30c9\u3001\u53ce\u96c6\u3001\u30e1\u30ac\u30cd\u3001\u30c0\u30fc\u30c4\u3001\u30c0\u30a4\u30d3\u30f3\u30b0<\/td>\n<\/tr>\n
\u5065\u5eb7\u72b6\u614b<\/th>\n<\/tr>\n
\u732b\u30a2\u30ec\u30eb\u30ae\u30fc<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

\u7814\u7a76\u6210\u679c<\/h3>\n

\u96d1\u8a8c\u30ab\u30d0\u30fc\u30fb\u6249\u7d75<\/h4>\n
<\/a><\/a> <\/a> <\/a> <\/a> <\/a> <\/a> <\/a><\/center><\/div>\n

\u8ad6\u6587\u767a\u8868<\/h4>\n
[72] Masashi Mamada*<\/span><\/strong>, Satoshi Maedera, Susumu Oda, Thanh Ba Nguyen, Hajime Nakanotani, Takuji Hatakeyama, Chihaya Adachi*<\/div>\n
“Very low lasing threshold of DABNA derivatives with DFB structures”<\/div>\n
Mater. Chem. Front.<\/em>, 2022<\/strong>, in press.<\/div>\n
DOI:10.1039\/D2QM01040B<\/a><\/div>\n
<\/center><\/div>\n
[71] Monirul Hasan, Atul Shukla, Masashi Mamada<\/span><\/strong>, Chihaya Adachi, Shih-Chun Lo, Ebinazar B. Namdas*<\/div>\n
“Correlating exciton dynamics of thermally activated delayed-fluorescence emitters to efficiency roll-off in OLEDs”<\/div>\n
Phys. Rev. Applied<\/em>, 2022<\/strong>, 2022<\/strong>, 18<\/em>, 054082.<\/div>\n
DOI:10.1103\/PhysRevApplied.18.054082<\/a><\/div>\n
<\/center><\/div>\n
[70] Masashi Mamada*<\/span><\/strong>, Chihaya Adachi*<\/div>\n
“Unexpected role of hole and electron blocking interlayers controlling charge carrier injection and transport in TADF based blue organic light-emitting diodes”<\/div>\n
Appl. Phys. Lett.<\/em>, 2022<\/strong>, 121<\/em>, 131103.<\/div>\n
DOI:10.1063\/5.0100373<\/a><\/div>\n
<\/center><\/div>\n
[69] Chin-Yiu Chan*, Yi-Ting Lee, Masashi Mamada<\/span><\/strong>, Kenichi Goushi, Youichi Tsuchiya, Hajime Nakanotani, Chihaya Adachi*<\/div>\n
“Carbazole-2-carbonitrile as an acceptor in deep-blue thermally activated delayed fluorescence emitters for narrowing charge-transfer emissions”<\/div>\n
Chem. Sci.<\/em>, 2022<\/strong>, 13<\/em>, 7821\u20137828.<\/div>\n
DOI:10.1039\/D2SC02478K<\/a><\/div>\n
<\/center><\/div>\n
[68] Yi-Ting Lee, Chin-Yiu Chan*, Masaki Tanaka, Masashi Mamada<\/span><\/strong>, Kenichi Goushi, Xun Tang, Youichi Tsuchiya, Hajime Nakanotani, Chihaya Adachi*<\/div>\n
“Tailor-made Multi-Resonance Terminal Emitters Towards Narrowband, High-Efficiency, and Stable Hyperfluorescence Organic Light-Emitting Diodes”<\/div>\n
Adv. Opt. Mater.<\/em>, 2022<\/strong>, 2200682.<\/div>\n
DOI:10.1002\/adom.202200682<\/a><\/div>\n
<\/center><\/div>\n
[67] Masashi Mamada*<\/span><\/strong>, Hiroshi Katagiri, Chin-Yiu Chan, Yi-Ting Lee, Kenichi Goushi, Hajime Nakanotani, Takuji Hatakeyama, Chihaya Adachi*<\/div>\n
“Highly Efficient Deep-Blue Organic Light-Emitting Diodes Based on Rational Molecular Design and Device Engineering”<\/div>\n
Adv. Funct. Mater.<\/em>, 2022<\/strong>, 2204352.<\/div>\n
DOI:10.1002\/adfm.202204352<\/a><\/div>\n
<\/center><\/div>\n
[66] Tanguy Jousselin-Oba, Masashi Mamada<\/span><\/strong>, Karen Wright, J\u00e9rome Marrot, Chihaya Adachi, Abderrahim Yassar, Michel Frigoli*<\/div>\n
“Synthesis, Crystal Structure, Tropicity and Charge Transport Properties of Diindenothienothiophene Derivatives”<\/div>\n
J. Mater. Chem. C<\/em>, 2022<\/strong>, 10<\/em>, 7717\u20137723.<\/div>\n
DOI:10.1039\/D2TC01324J<\/a><\/div>\n
<\/center><\/div>\n
[65] Nicholle R. Wallwork, Masashi Mamada*<\/span><\/strong>, Angus B. Keto, Sarah K. M. McGregor, Atul Shukla, Chihaya Adachi, Elizabeth Krenske, Ebinazar B. Namdas*, Shih-Chun Lo*<\/div>\n
“Cibalackrot Dendrimers for Hyperfluorescent Organic Light-Emitting Diodes”<\/div>\n
Macromol. Rapid Commun.<\/em>, 2022<\/strong>, 2200118.<\/div>\n
DOI:10.1002\/marc.202200118<\/a><\/div>\n
<\/center><\/div>\n
[64] Atul Shukla*, Volter Entoma, Sarah K. M. McGregor, Monirul Hasan, Masashi Mamada<\/span><\/strong>, Evan G. Moore, Chihaya Adachi, Shih-Chun Lo*, Ebinazar B. Namdas*<\/div>\n
“Low Light Amplification Threshold and Reduced Efficiency Roll-Off in Thick Emissive Layer OLEDs from a Diketopyrrolopyrrole Derivative”<\/div>\n
Macromol. Rapid Commun.<\/em>, 2022<\/strong>, 2200115.<\/div>\n
DOI:10.1002\/marc.202200115<\/a><\/div>\n
<\/center><\/div>\n
[63] Ayano Abe, Kenichi Goushi*, Atula S. D. Sandanayaka, Ryutaro Komatsu, Takashi Fujihara, Masashi Mamada<\/span><\/strong>, Chihaya Adachi*<\/div>\n
“Numerical Study of Triplet Dynamics in Organic Semiconductors Aimed for the Active Utilization of Triplets by TADF under Continuous-Wave Lasing”<\/div>\n
J. Phys. Chem. Lett.<\/em>, 2022<\/strong>, 13<\/em>, 1323\u20131329.<\/div>\n
DOI:10.1021\/acs.jpclett.1c03983<\/a><\/div>\n
<\/center><\/div>\n
[62] Nicholle R. Wallwork, Masashi Mamada*<\/span><\/strong>, Atul Shukla, Sarah K. M. McGregor, Chihaya Adachi*, Ebinazar Namdas*, Shih-Chun Lo*<\/div>\n
“High-Performance Solution Processed Red Hyperfluorescent OLEDs Based on Cibalackrot”<\/div>\n
J. Mater. Chem. C<\/em>, 2022<\/strong>, 10<\/em>, 4767\u20134774.<\/div>\n
DOI:10.1039\/D1TC04937B<\/a><\/div>\n
<\/center><\/div>\n
[61] Tomohiro Ishii, Kiyoshi Miyata, Masashi Mamada<\/span><\/strong>, Fatima Bencheikh, Fabrice Mathevet, Ken Onda, St\u00e9phane K\u00e9na-Cohen, Chihaya Adachi*<\/div>\n
“Low-threshold exciton-polariton condensation via fast polariton relaxation in organic microcavities”<\/div>\n
Adv. Opt. Mater.<\/em>, 2022<\/strong>, 10<\/em>, 2102034.<\/div>\n
DOI:10.1002\/adom.202102034<\/a><\/div>\n
<\/center><\/div>\n
[60] Tanguy Jousselin-Oba, Masashi Mamada*<\/span><\/strong>, Karen Wright, J\u00e9rome Marrot, Chihaya Adachi, Abderrahim Yassar, Michel Frigoli*<\/div>\n
“Synthesis, Aromaticity and Application of peri-PentacenoPentacene: Localized Representation of Benzenoid Aromatic Compounds”<\/div>\n
Angew. Chem. Int. Ed.<\/em>, 2022<\/strong>, 61<\/em>, e202112794.<\/div>\n
DOI:10.1002\/anie.202112794<\/a><\/div>\n
<\/center><\/div>\n
[59] Masashi Mamada*<\/span><\/strong>, Hajime Nakanotani, Chihaya Adachi*<\/div>\n
“Amplified spontaneous emission from oligo(p-phenylenevinylene) derivatives”<\/div>\n
Mater. Adv.<\/em>, 2021<\/strong>, 2<\/em>, 3906\u20133914.<\/div>\n
DOI:10.1039\/D0MA00756K<\/a><\/div>\n
<\/center><\/div>\n
[58] Yi-Ting Lee, Chin-Yiu Chan, Masaki Tanaka, Masashi Mamada<\/span><\/strong>, Umamahesh Balijapalli, Youichi Tsuchiya, Hajime Nakanotani, Takuji Hatakeyama, Chihaya Adachi*<\/div>\n
“Investigating HOMO Energy Levels of Terminal Emitters for Realizing High-Brightness and Stable TADF-Assisted Fluorescence Organic Light-Emitting Diodes”<\/div>\n
Adv. Electron. Mater.<\/em>, 2021<\/strong>, 7<\/em>, 2001090.<\/div>\n
DOI:10.1002\/aelm.202001090<\/a><\/div>\n
<\/center><\/div>\n
[57] Yuya Oyama, Masashi Mamada*<\/span><\/strong>, Akihiro Kondo*, Chihaya Adachi*<\/div>\n
“Advantages of naphthalene as building block for organic solid state laser dyes: Smaller energy gaps and enhanced stability”<\/div>\n
J. Mater. Chem. C<\/em>, 2021<\/strong>, 9<\/em>, 4112\u20134118.<\/div>\n
DOI:10.1039\/D0TC05387B<\/a><\/div>\n
Selected as the outside front cover picture <\/span>[image]<\/a><\/div>\n
<\/center><\/div>\n
[56] Xuelong Liu, Chin-Yiu Chan*, Fabrice Mathevet, Masashi Mamada<\/span><\/strong>, Youichi Tsuchiya, Yi-Ting Lee, Hajime Nakanotani, Shinichiro Kobayashi, Masayuki Shiochi, Chihaya Adachi*<\/div>\n
“Isotope Effect of Host Material on Device Stability of Thermally Activated Delayed Fluorescence Organic Light-Emitting Diodes”<\/div>\n
Small Sci.<\/em>, 2021<\/strong>, 1<\/em>, 2000057.<\/div>\n
DOI:10.1002\/smsc.202000057<\/a><\/div>\n
<\/center><\/div>\n
[55] Masashi Mamada*<\/span><\/strong>, Kenichi Goushi*, Ryota Nakamura, Hironori Kaji, Chihaya Adachi*<\/div>\n
“Synthesis and Characterization of 5,5′-Bitetracene”<\/div>\n
Chemistry Letters<\/em>, 2021<\/strong>, 50<\/em>, 800\u2013803.<\/div>\n
DOI:10.1246\/cl.200909<\/a><\/div>\n
<\/center><\/div>\n
[54] Yuto Kage, Seongsoo Kang, Shigeki Mori, Masashi Mamada*<\/span><\/strong>, Chihaya Adachi, Dongho Kim*, Hiroyuki Furuta*, Soji Shimizu*<\/div>\n
“An Electron-Accepting aza-BODIPY-Based Donor\u2013Acceptor\u2013Donor Architecture for Bright NIR Emission”<\/div>\n
Chem. Eur. J.<\/em>, 2021<\/strong>, 27<\/em>, 5259\u20135267.<\/div>\n
DOI:10.1002\/chem.202005360<\/a><\/div>\n
Selected as a Very Important Paper <\/span><\/div>\n
<\/center><\/div>\n
[53] Umamahesh Balijapalli, Ryo Nagata, Nishiki Yamada, Hajime Nakanotani*, Masaki Tanaka, Anthony D’Al\u00e9o, Virginie Placide, Masashi Mamada<\/span><\/strong>, Youichi Tsuchiya*, Chihaya Adachi*<\/div>\n
“Highly Efficient Near-Infrared Electrofluorescence from a Thermally-Activated Delayed Fluorescence Molecule”<\/div>\n
Angew. Chem. Int. Ed.<\/em>, 2021<\/strong>, 60<\/em>, 8477\u20138482.<\/div>\n
DOI:10.1002\/anie.202016089<\/a><\/div>\n
Selected as a Hot Paper <\/span><\/div>\n
<\/center><\/div>\n
[52] Reiko Aoki, Ryutaro Komatsu, Kenichi Goushi, Masashi Mamada*<\/span><\/strong>, Soo Young Ko, Jeong Weon Wu, Virginie Placide, Anthony D\u2019Al\u00e9o*, Chihaya Adachi*<\/div>\n
“Realizing Near-Infrared Laser Dyes through a Shift in Excited-State Absorption”<\/div>\n
Advanced Optical Materials<\/em>, 2021<\/strong>, 9<\/em>, 2001947.<\/div>\n
DOI:10.1002\/adom.202001947<\/a><\/div>\n
Selected as the outside front cover picture <\/span>[image]<\/a><\/div>\n
<\/center><\/div>\n
[51] Van Mai, Viqar Ahmad, Masashi Mamada<\/span><\/strong>, Toshiya Fukunaga, Atul Shukla, Jan Sobus, Gowri Krishnan, Evan Moore, Gunther Andersson, Chihaya Adachi*, Ebinazar Namdas*, Shih-Chun Lo<\/div>\n
“Solid cyclooctatetraene-based triplet quencher demonstrating excellent suppression of singlet\u2013triplet annihilation in optical and electrical excitation”<\/div>\n
Nature Communications<\/em>, 2020<\/strong>, 11<\/em>, 5623.<\/div>\n
DOI:10.1038\/s41467-020-19443-z<\/a><\/div>\n
<\/center><\/div>\n
[50] Masashi Mamada*<\/span><\/strong>, Ryota Nakamura, Chihaya Adachi*<\/div>\n
“Synthesis, crystal structure and charge transport characteristics of stable peri-tetracene analogues”<\/div>\n
Chemical Science<\/em>, 2021<\/strong>, 12<\/em>, 552\u2013558.<\/div>\n
DOI:10.1039\/D0SC04699J<\/a><\/div>\n
Selected as the inside front cover picture <\/span>[image]<\/a><\/div>\n
<\/center><\/div>\n
[49] Tanguy Jousselin-Oba, Masashi Mamada*<\/span><\/strong>, Atsushi Okazawa, J\u00e9rome Marrot, Takayuki Ishida, Chihaya Adachi, Abderrahim Yassar, Michel Frigoli*<\/div>\n
“Modulating the ground state, stability and charge transport in OFETs of biradicaloid Hexahydro-diindenopyrene derivatives and a proposed method to estimate the biradical character”<\/div>\n
Chemical Science<\/em>, 2020<\/strong>, 11<\/em>, 12194\u201312205.<\/div>\n
DOI:10.1039\/D0SC04583G<\/a><\/div>\n
<\/center><\/div>\n
[48] Kentaro Yamamoto, Daisuke Kawaguchi*, Tatsuki Abe, Takeshi Komino, Masashi Mamada<\/span><\/strong>, Taizo Kabe, Chihaya Adachi, Kensuke Naka, Keiji Tanaka*<\/div>\n
“Surface Segregation of Star-Shaped Polyhedral Oligomeric Silsesquioxane in Polymer Matrix”<\/div>\n
Langmuir<\/em>, 2020<\/strong>, 36<\/em>, 9960\u20139966.<\/div>\n
DOI:10.1021\/acs.langmuir.0c01785<\/a><\/div>\n
<\/center><\/div>\n
[47] Michel Frigoli*, Tanguy Jousselin-Oba, Masashi Mamada<\/span><\/strong>, J\u00e9r\u00f4me Marrot, Agnese Zangarelli, Danilo Pannacci, Chihaya Adachi, Fausto Ortica*<\/div>\n
“Synthesis and photochromic behaviour of a series of benzopyrans bearing an N-phenyl-carbazole moiety: photochromism control by the steric effect”<\/div>\n
Photochem. Photobiol. Sci.<\/em>, 2020<\/strong>, 19<\/em>, 1344\u20131355.<\/div>\n
DOI:10.1039\/D0PP00202J<\/a><\/div>\n
<\/center><\/div>\n
[46] Viqar Ahmad, Jan Sobus, Fatima Bencheikh, Masashi Mamada<\/span><\/strong>, Chihaya Adachi, Shih-Chun Lo*, Ebinazar B. Namdas*<\/div>\n
“High EQE and high brightness solution-processed TADF light-emitting transistors and OLEDs”<\/div>\n
Adv. Opt. Mater.<\/em>, 2020<\/strong>, 202000554.<\/div>\n
DOI:10.1002\/adom.202000554<\/a><\/div>\n
<\/center><\/div>\n
[45] Monirul Hasan, Atul Shukla, Viqar Ahmad, Jan Sobus, Fatima Bencheikh, Sarah M. K. McGregor, Masashi Mamada<\/span><\/strong>, Chihaya Adachi*, Shih-Chun Lo*, Ebinazar B. Namdas*<\/div>\n
“Exciton-exciton annihilation in thermally activated delayed fluorescence emitter”<\/div>\n
Adv. Funct. Mater.<\/em>, 2020<\/strong>, 30<\/em>, 2000580.<\/div>\n
DOI:10.1002\/adfm.202000580<\/a><\/div>\n
<\/center><\/div>\n
[44] Masashi Mamada*<\/span><\/strong>, Ryutaro Komatsu, Chihaya Adachi*<\/div>\n
“F8BT Oligomers for Organic Solid-State Lasers”<\/div>\n
ACS Appl. Mater. Interfaces<\/em>, 2020<\/strong>, 12<\/em>, 28383\u201328391.<\/div>\n
DOI:10.1021\/acsami.0c05449<\/a><\/div>\n
<\/center><\/div>\n
[43] Yun Long, Masashi Mamada<\/span><\/strong>, Chunyong Li, Paloma Lays dos Santos, Marco Colella, Andrew Danos, Chihaya Adachi, Andrew P. Monkman*<\/div>\n
“Excited State Dynamics of Thermally Activated Delayed Fluorescence from an Excited State Intramolecular Proton Transfer System”<\/div>\n
J. Phys. Chem. Lett.<\/em> 2020<\/strong>, 11<\/em>, 3305\u20133312.<\/div>\n
DOI:10.1021\/acs.jpclett.0c00498<\/a><\/div>\n
<\/center><\/div>\n
\u00a0<\/div>\n
[42] Yuya Oyama, Masashi Mamada*<\/span><\/strong>, Atul Shukla, Evan G. Moore, Shih-Chun Lo, Ebinazar B. Namdas and Chihaya Adachi*<\/div>\n
“Design strategy for robust organic semiconductor laser dyes”<\/div>\n
ACS. Mater. Lett.<\/em> 2020<\/strong>, 2<\/em>, 161\u2013167.<\/div>\n
DOI:10.1021\/acsmaterialslett.9b00536<\/a><\/div>\n
<\/center><\/div>\n
[41] Paulius Baronas*, Gediminas Kreiza, Masashi Mamada<\/span><\/strong>, Satoshi Maedera, Povilas Adom\u0117nas, Ona Adom\u0117nien\u0117, Karolis Kazlauskas, Chihaya Adachi, Saulius Jur\u0161\u0117nas*<\/div>\n
“Enhanced energy transfer in doped bifluorene single crystals: prospects for organic lasers”<\/div>\n
Adv. Opt. Mater.<\/em> 2020<\/strong>, 8<\/em>, 1901670.<\/div>\n
DOI:10.1002\/adom.201901670<\/a><\/div>\n
<\/center><\/div>\n
[40] Tanguy Jousselin-Oba, Masashi Mamada*<\/span><\/strong>, J\u00e9r\u00f4me Marrot, Antoine Maignan, Chihaya Adachi, Abderrahim Yassar, and Michel Frigoli*<\/div>\n
“Excellent Semiconductors Based on Tetracenotetracene and Pentacenopentacene: From Stable Closed-Shell to Singlet Open-Shell”<\/div>\n
J. Am. Chem. Soc.<\/em> 2019<\/strong>, 141<\/em>, 9373\u20139381.<\/div>\n
DOI:10.1021\/jacs.9b03488<\/a><\/div>\n
<\/center><\/div>\n
[39] Yi-Ting Lee, Po-Chen Tseng, Takeshi Komino, Masashi Mamada<\/span><\/strong>, Ruby Janet Ortiz, Man-kit Leung, Tien-Lung Chiu, Chi-Feng Lin, Jiun-Haw Lee*, Chihaya Adachi*, Chao-Tsen Chen*, Chin-Ti Chen*<\/div>\n
“Simple molecular-engineering approach for enhancing orientation and out-coupling efficiency of thermally activated delayed fluorescent emitters without red-shifting emission”<\/div>\n
ACS Appl. Mater. Interfaces<\/em>, 2018<\/strong>, 10<\/em>, 43842\u201343849.<\/div>\n
DOI:10.1021\/acsami.8b16199<\/a><\/div>\n
<\/center><\/div>\n
[38] Van T. N. Mai, Atul Shukla, Masashi Mamada<\/span><\/strong>, Satoshi Maedera, Paul E. Shaw, Jan Sobus, Ilene Allison, Chihaya Adachi*, Ebinazar B. Namdas*, Shih-Chun Lo*<\/div>\n
“Low ASE Threshold and Efficient Electroluminescence from a Carbazole Derivatized Excited State Intramolecular Proton Transfer (ESIPT) Dye”<\/div>\n
ACS Photonics<\/em>, 2018<\/strong>, 5<\/em>, 4447\u20134455<\/div>\n
DOI:10.1021\/acsphotonics.8b00907<\/a><\/div>\n
Selected as a supplementary cover picture <\/span>[image]<\/a><\/div>\n
<\/center><\/div>\n
[37] Masashi Mamada*<\/span><\/strong>, Guojian Tian, Hajime Nakanotani, Jianhua Su, Chihaya Adachi*<\/div>\n
“The Importance of Excited\u2010State Energy Alignment for Efficient Exciplex Systems Based on a Study of Phenylpyridinato Boron Derivatives”<\/div>\n
Angew. Chem. Int. Ed.<\/em>, 2018<\/strong>, 57<\/em>, 12380\u201312384<\/div>\n
DOI:10.1002\/anie.201804218<\/a><\/div>\n
<\/center><\/div>\n
[36] Masashi Mamada*<\/span><\/strong>, Toshiya Fukunaga, Fatima Bencheikh, Atula S. D. Sandanayaka, Chihaya Adachi*<\/div>\n
“Low Amplified Spontaneous Emission Threshold from Organic Dyes Based on Bis-stilbene”<\/div>\n
Adv. Funct. Mater.<\/em>, 2018<\/strong>, 28<\/em>, 1802130<\/div>\n
DOI:10.1002\/adfm.201802130<\/a><\/div>\n
<\/center><\/div>\n
[35] Jan Sobus, Fatima Bencheikh, Masashi Mamada<\/span><\/strong>, Robert Wawrzinek, Jean-Charles Ribierre, Chihaya Adachi*, Shih-Chun Lo*, Ebinazar B. Namdas*<\/div>\n
“High performance p-and n-type light-emitting field-effect transistors employing thermally activated delayed fluorescence”<\/div>\n
Adv. Funct. Mater.<\/em>, 2018<\/strong>, 28<\/em>, 1800340<\/div>\n
DOI:10.1002\/adfm.201800340<\/a><\/div>\n
<\/center><\/div>\n
[34] Masashi Mamada*<\/span><\/strong>, Tsuyoshi Minami*, Hiroshi Katagiri, Takafumi Omiya, Shizuo Tokito<\/div>\n
“One-step, green synthesis of a supramolecular organogelator based on mellitic triimide for the recognition of aromatic compounds”<\/div>\n
Chem. Commun.<\/em>, 2017<\/strong>, 53<\/em>, 8834\u20138837<\/div>\n
DOI:10.1039\/C7CC04876A<\/a><\/div>\n
Selected as a back cover picture <\/span>[image]<\/a><\/div>\n
<\/center><\/div>\n
[33] Masashi Mamada*<\/span><\/strong>, Ko Inada, Takeshi Komino, William J. Potscavage, Jr., Hajime Nakanotani, Chihaya Adachi*<\/div>\n
“Highly Efficient Thermally Activated Delayed Fluorescence from an Excited-State Intramolecular Proton Transfer System”<\/div>\n
ACS Cent. Sci.<\/em>, 2017<\/strong>, 3<\/em>, 769\u2013777<\/div>\n
DOI:10.1021\/acscentsci.7b00183<\/a><\/div>\n
<\/center><\/div>\n
[32] Yuta Ogawa, Kazuhiro Yamamoto, Chiyo Miura, Shigeki Tamura, Mitsuki Saito, Masashi Mamada<\/span><\/strong>, Daisuke Kumaki, Shizuo Tokito, Hiroshi Katagiri*<\/div>\n
“Asymmetric Alkylthienyl Thienoacenes Derived from Anthra[2,3-b]thieno[2,3-d]thiophene for Solution-Processable Organic Semiconductors”<\/div>\n
ACS Appl. Mater. Interfaces <\/em>2017<\/strong>, 9<\/em>, 9902\u20139909<\/div>\n
DOI:10.1021\/acsami.6b15793<\/a><\/div>\n
<\/center><\/div>\n
[31] Kamal Sbargoud, Masashi Mamada*<\/span><\/strong>, Tanguy Jousselin-Oba, Yasunori Takeda, Shizuo Tokito, Abderrahim Yassar, J\u00e9r\u00f4me Marrot, Michel Frigoli*<\/div>\n
“Low-Band Gap Bistetracene-Based Organic Semiconductors Exhibiting Air Stability, High Aromaticity and Mobility”<\/div>\n
Chem. Eur. J. <\/em>2017<\/strong>, 23<\/em>, 5076\u20135080<\/div>\n
DOI:10.1002\/chem.201605906<\/a><\/div>\n
<\/center><\/div>\n
[30] Yuta Ogawa, Erika Takiguchi, Masashi Mamada<\/span><\/strong>, Daisuke Kumaki, Shizuo Tokito, Hiroshi Katagiri*
\n“Synthesis, crystal structure, and FET characteristics of thieno[2,3-b]thiophene-based bent-thienoacenes”<\/div>\n
Tetrahedron Lett. <\/em>2017<\/strong>, 58<\/em>, 963\u2013967<\/div>\n
DOI:10.1016\/j.tetlet.2017.01.074<\/a><\/div>\n
<\/center><\/div>\n
[29] Masashi Mamada*<\/span><\/strong>, Hiroshi Katagiri, Tomo Sakanoue, Shizuo Tokito<\/div>\n
“Crystal Structure and Theoretical Investigation of Charge Transport Properties of Fullerene Derivatives”<\/div>\n
Chem. Lett. <\/em>2016<\/strong>, 45<\/em>,1421\u20131424<\/div>\n
DOI:10.1246\/cl.160802<\/a><\/div>\n
Editor\u2019s Choice article<\/span><\/div>\n
<\/center><\/div>\n
[28] Masataka Ikeshima, Masashi Mamada<\/span><\/strong>, Tsuyoshi Minami, Shizuo Tokito, Shuji Okada*<\/div>\n
“Synthesis and solid-state polymerization of diacetylene derivatives directly substituted with a phenylcarbazole moiety”<\/div>\n
Polym. J.<\/em> 2016<\/strong>, 48<\/em>, 1013\u20131018<\/div>\n
DOI:10.1038\/pj.2016.67<\/a><\/div>\n
Selected as a cover picture<\/span><\/div>\n
<\/center><\/div>\n
[27] Yasunori Takeda, Kazuma Hayasaka, Rei Shiwaku, Koji Yokosawa, Takeo Shiba, Masashi Mamada<\/span><\/strong>, Daisuke Kumaki, Kenjiro Fukuda, Shizuo Tokito*<\/div>\n
“Fabrication of Ultra-Thin Printed Organic TFT CMOS Logic Circuits Optimized for Low-Voltage Wearable Sensor Applications”<\/div>\n
Sci. Rep.<\/em> 2016<\/strong>, 6<\/em>, 25714<\/div>\n
DOI:10.1038\/srep25714<\/a><\/div>\n
<\/center><\/div>\n
[26] Masashi Mamada*<\/span><\/strong>, Harunori Fujita, Kazuaki Kakita, Hidetaka Shima, Yasuhiro Yoneda, Yasuhiro Tanaka*, Shizuo Tokito<\/div>\n
“Crystal structure and modeled charge carrier mobility of benzobis(thiadiazole) derivatives”<\/div>\n
New J. Chem.<\/em> 2016<\/strong>, 40<\/em>, 1403\u20131411.<\/div>\n
DOI:10.1039\/c5nj02302e<\/a><\/div>\n
<\/center><\/div>\n
[25] Makoto Mizukami*, Shinya Oku, Seung-Il Cho, Masahiro Tatetsu, Miho Abiko, Masashi Mamada<\/span><\/strong>, Tomo Sakanoue, Yoshiyuki Suzuri, Junji Kido, Shizuo Tokito*<\/div>\n
“A Solution-Processed Organic Thin-Film Transistor Backplane for Flexible Multiphoton Emission Organic Light-Emitting Diode Displays”<\/div>\n
IEEE Electron Device Lett.<\/em> 2015<\/strong>, 36<\/em>, 841\u2013843.<\/div>\n
DOI:10.1109\/LED.2015.2443184<\/a><\/div>\n
<\/center><\/div>\n
[24] Kamal Sbargoud, Masashi Mamada*<\/span><\/strong>, J\u00e9r\u00f4me Marrot, Shizuo Tokito, Abderrahim Yassar*, Michel Frigoli*<\/div>\n
“Diindeno[1,2-b:2′,1′-n]Perylene: a Closed Shell related Chichibabin\u2019s Hydrocarbon, Synthesis, Molecular Packing, Electronic and Charge Transport Properties”<\/div>\n
Chem. Sci.<\/em> 2015<\/strong>, 6<\/em>, 3402\u20133409.<\/div>\n
DOI: 10.1039\/C5SC00652J<\/a><\/div>\n
<\/center><\/div>\n
[23] Masataka Ikeshima, Masashi Mamada<\/span><\/strong>, Hiroshi Katagiri, Tsuyoshi Minami, Shuji Okada, Shizuo Tokito*<\/div>\n
“Synthesis and Solid-State Polymerization of Diacetylene Derivatives with an N-Carbazolylphenyl Group”<\/div>\n
Bull. Chem. Soc. Jpn.<\/em> 2015<\/strong>, 88<\/em>, 843\u2013849.<\/div>\n
DOI:10.1246\/bcsj.20150019<\/a><\/div>\n
<\/center><\/div>\n
[22] Masashi Mamada<\/span><\/strong>, Hidetaka Shima, Yasuhiro Yoneda, Tetsuro Shimano, Natsuko Yamada, Kazuaki Kakita, Toshikazu Machida, Yasuhiro Tanaka*, Sei Aotsuka, Daisuke Kumaki, Shizuo Tokito*<\/div>\n
“A Unique Solution Processable n-Type Semiconductor Material Design for High Performance Organic Field-Effect Transistors”<\/div>\n
Chem. Mater.<\/em> 2015<\/strong>, 27<\/em>, 141\u2013147.<\/div>\n
DOI:10.1021\/cm503579m<\/a><\/div>\n
<\/center><\/div>\n
[21] Masashi Mamada*<\/span><\/strong>, Hiroshi Katagiri, Tomo Sakanoue, Shizuo Tokito<\/div>\n
“Characterization of New Rubrene Analogues with Heteroaryl-Substituents”<\/div>\n
Cryst. Growth Des.<\/em> 2015<\/strong>, 15<\/em>, 442\u2013448.<\/div>\n
DOI:10.1021\/cg501519a<\/a><\/div>\n
<\/center><\/div>\n
[20] Masashi Mamada<\/span><\/strong>, C\u00e9sar Perez-Bolivar, Daisuke Kumaki, Nina A. Esipenko, Shizuo Tokito, Pavel Anzenbacher, Jr.*<\/div>\n
“Benzimidazole Derivatives: Synthesis, Physical Properties, and n-Type Semiconducting Properties”<\/div>\n
Chem. Eur. J.<\/em> 2014<\/strong>, 20<\/em>, 11835\u201311846.<\/div>\n
DOI:10.1002\/chem.201403058<\/a><\/div>\n
<\/center><\/div>\n
[19] Masashi Mamada*<\/span><\/strong>, Taisuke Uemura, Ryo Teraoka, Daisuke Kumaki, Shizuo Tokito<\/div>\n
“Synthesis of Narrow Bandgap Polymers based on Benzobis(thiadiazole) and their Application to Organic Transistor Devices”<\/div>\n
J. Photopolym. Sci.<\/em> 2014<\/strong>, 27<\/em>, 321\u2013326.<\/div>\n
DOI:10.2494\/photopolymer.27.321<\/a><\/div>\n
<\/center><\/div>\n
[18] Taisuke Uemura, Masashi Mamada*<\/span><\/strong>, Ryo Teraoka, Daisuke Kumaki, Shizuo Tokito*<\/div>\n
“Synthesis and Thin-Film Transistor Characterization of Narrow-Gap N-type Semiconducting Polymers based on Benzobis(thiadiazole)”<\/div>\n
Chem. Lett.<\/em> 2014<\/strong>, 43<\/em>, 402\u2013404.<\/div>\n
DOI:10.1246\/cl.131025<\/a><\/div>\n
<\/center><\/div>\n
[17] Masashi Mamada*<\/span><\/strong>, Hiroshi Katagiri, Makoto Mizukami, Kota Honda, Tsukuru Minamiki, Ryo Teraoka, Taisuke Uemura, Shizuo Tokito<\/div>\n
“syn-\/anti-Anthradithiophene Derivative Isomer Effects on Semiconducting Properties”<\/div>\n
ACS Appl. Mater. Interfaces<\/em> 2013<\/strong>, 5<\/em>, 9670\u20139677.<\/div>\n
DOI:10.1021\/am4027136<\/a><\/div>\n
<\/center><\/div>\n
[16] Taisuke Uemura, Masashi Mamada<\/span><\/strong>, Daisuke Kumaki, Shizuo Tokito*<\/div>\n
“Synthesis of Semiconducting Polymers through Soluble Precursor Polymers with Thermally Removable Groups and Their Application to Organic Transistors”<\/div>\n
ACS Macro Lett.<\/em> 2013<\/strong>, 2<\/em>, 830\u2013833.<\/div>\n
DOI:10.1021\/mz400328r<\/a><\/div>\n
<\/center><\/div>\n
[15] Masashi Mamada*<\/span><\/strong>, Tsukuru Minamiki, Hiroshi Katagiri, Shizuo Tokito*<\/div>\n
“Synthesis, Physical Properties, and Field-Effect Mobility of Isomerically Pure syn-\/anti-Anthradithiophene Derivatives”<\/div>\n
Org. Lett.<\/em> 2012<\/strong>, 14<\/em>, 4062\u20134065.<\/div>\n
DOI:10.1021\/ol301626u<\/a><\/div>\n
<\/center><\/div>\n
[14] Masashi Mamada<\/span><\/strong>, C\u00e9sar P\u00e9rez-Bol\u00edvar, Pavel Anzenbacher, Jr.*<\/div>\n
“Green Synthesis of Polycyclic Benzimidazole Derivatives and Organic Semiconductors”<\/div>\n
Org. Lett.<\/em> 2011<\/strong>, 13<\/em>, 4882\u20134885.<\/div>\n
DOI:10.1021\/ol201973w<\/a><\/div>\n
<\/center><\/div>\n
[13] Masashi Mamada<\/span><\/strong>, Selin Ergun, C\u00e9sar P\u00e9rez-Bol\u00edvar, Pavel Anzenbacher, Jr.<\/div>\n
“Charge transport, carrier balance, and blue electrophosphorescence in diphenyl[4-(triphenylsilyl)phenyl]-phosphine oxide devices.”<\/div>\n
Appl. Phys. Lett.<\/em> 2011<\/strong>, 98<\/em>, 073305.<\/div>\n
DOI:10.1063\/1.3555335<\/a><\/div>\n
<\/center><\/div>\n
[12] Masashi Mamada<\/span><\/strong>, Daisuke Kumaki, Jun-ichi Nishida, Shizuo Tokito, Yoshiro Yamashita*<\/div>\n
“Novel Semiconducting Quinone for Air-Stable n-Type Organic Field-Effect Transistors.”<\/div>\n
ACS Appl. Mater. Interfaces<\/em> 2010<\/strong>, 2<\/em>, 1303\u20131307.<\/div>\n
DOI:10.1021\/am1001794<\/a><\/div>\n
<\/center><\/div>\n
[11] Keiko Omata, Masashi Mamada<\/span><\/strong>, Jun-ichi Nishida, Shizuo Tokito, Yoshiro Yamashita<\/div>\n
“Organic Field-Effect Transistors Based on \u03c0-Extended Dibenzotetrathiafulvalene Analogues with Thiophene Spacers.”<\/div>\n
Bull. Chem. Soc. Jpn.<\/em> 2010<\/strong>, 83<\/em>, 575\u2013581.<\/div>\n
DOI:10.1246\/bcsj.20090290<\/a><\/div>\n
<\/center><\/div>\n
[10] Yoshihide Fujisaki*, Masashi Mamada<\/span><\/strong>, Daisuke Kumaki, Shizuo Tokito, Yoshiro Yamashita<\/div>\n
“Low-Voltage and Hysteresis-Free N-Type Organic Thin Film Transistor and Complementary Inverter with Bilayer Gate Insulator.”<\/div>\n
Jpn. J. Appl. Phys.<\/em> 2009<\/strong>, 48<\/em>, 111504.<\/div>\n
DOI:10.1143\/JJAP.48.111504<\/a><\/div>\n
<\/center><\/div>\n
[9] Altanbolag, Masashi Mamada<\/span><\/strong>, Jun-ichi Nishida, Yoshiro Yamashita*<\/div>\n
“Field-Effect Transistors Based on Tetraphenyl-dipyranylidenes and the Sulfur Analogues.”<\/div>\n
Chem. Mater.<\/em> 2009<\/strong>, 21<\/em>, 4350\u20134352.<\/div>\n
DOI:10.1021\/cm902037w<\/a><\/div>\n
<\/center><\/div>\n
[8] Masashi Mamada<\/span><\/strong>, Yoshiro Yamashita*<\/div>\n
“Triclinic Polymorph of Dibenzotetrathiafulvalene.”<\/div>\n
Acta Crystallogr. Sect. E<\/em> 2009<\/strong>, 65<\/em>, o2083.<\/div>\n
DOI:10.1107\/S1600536809030013<\/a><\/div>\n
<\/center><\/div>\n
[7] Masashi Mamada<\/span><\/strong>, Jun-ichi Nishida, Shiuo Tokito, Yoshiro Yamashita*<\/div>\n
“Anthraquinone Derivatives Affording n-Type Organic Thin Film Transistors.”<\/div>\n
Chem. Commun.<\/em> 2009<\/strong>, 16<\/em>, 2177\u20132179.<\/div>\n
DOI:10.1039\/B820520E<\/a><\/div>\n
<\/center><\/div>\n
[6] Masashi Mamada<\/span><\/strong>, Jun-ichi Nishida, Shizuo Tokito, Yoshiro Yamashita*<\/div>\n
“Preparation, Characterization, and Field-effect Transistor Performance of Benzo[1,2-d:4,5-d’]bisthiazole Derivatives.”<\/div>\n
Chem. Lett.<\/em> 2008<\/strong>, 37<\/em>, 766\u2013767.<\/div>\n
DOI:10.1246\/cl.2008.766<\/a><\/div>\n
<\/center><\/div>\n
[5] Masashi Mamada<\/span><\/strong>, Jun-ichi Nishida, Daisuke Kumaki, Shizuo Tokito, Yoshiro Yamashita*<\/div>\n
“High Performance Organic Field-Effect Transistors Based on [2,2′]Bi[naphtho[2,3-b]thiophenyl] with a Simple Structure.”<\/div>\n
J. Mater. Chem.<\/em> 2008<\/strong>, 18<\/em>, 3442\u20133447.<\/div>\n
DOI:10.1039\/B801425F<\/a><\/div>\n
<\/center><\/div>\n
[4] Masashi Mamada<\/span><\/strong>, Jun-ichi Nishida, Daisuke Kumaki, Shizuo Tokito, Yoshiro Yamashita*<\/div>\n
“n-Type Organic Field-Effect Transistors with High Electron Mobilities Based on Thiazole-thiazolothiazole Conjugated Molecules.”<\/div>\n
Chem. Mater.<\/em> 2007<\/strong>, 19<\/em>, 5404\u20135409.<\/div>\n
DOI:10.1021\/cm071505s<\/a><\/div>\n
<\/center><\/div>\n
[3] Susumu Tajima*, Daisuke Ishiguro, Masashi Mamada<\/span><\/strong>, Satoshi Nakajima<\/div>\n
“Unimolecular Reactions of Diethtyl Malonate Cation in Gas-phase.”<\/div>\n
J. Mass Spectrom. Soc. Jpn.<\/em> 2004<\/strong>, 52<\/em>, 263\u2013270.<\/div>\n
DOI:10.5702\/massspec.52.263<\/a><\/div>\n
<\/center><\/div>\n
[2] Susumu Tajima*, Masashi Mamada<\/span><\/strong>, Satoshi Nakajima, Yutaka Takahashi, Nico M. M. Nibbering<\/div>\n
“Unimolecular Gas-Phase Reactions of Diethyl Phthalate, Isophthalate, and Terephthalate upon Electron Ionization.”<\/div>\n
Aust. J. Chem.<\/em> 2003<\/strong>, 56<\/em>, 473\u2013479.<\/div>\n
DOI:10.1071\/CH03077<\/a><\/div>\n
<\/center><\/div>\n
[1] Susumu Tajima*, Shoko Kojima, Yuko Hiroi, Masashi Mamada<\/span><\/strong>, Satoshi Nakajima, Nico M. M. Nibbering<\/div>\n
“Unimolecular Metastable Decompositions of 1,1,1-Trifluoroisopropyl Methyl Ether upon Electron Ionization.”<\/div>\n
Rapid Commun. Mass Spectrom.<\/em> 2003<\/strong>, 17<\/em>, 503\u2013506.<\/div>\n
DOI:10.1002\/rcm.892<\/a><\/div>\n
<\/center><\/div>\n

\u8457\u66f8\u30fb\u89e3\u8aac\u30fb\u7dcf\u8aac\u7b49<\/h4>\n
\n
[3]<\/dt>\n
\u6709\u6a5f\u534a\u5c0e\u4f53\u30ec\u30fc\u30b6\u30fc\u5206\u5b50\u306e\u8010\u4e45\u7279\u6027\u306e\u5411\u4e0a
\n\u96fb\u6c17\u5b66\u4f1a\u8a8c<\/em>, 2021<\/strong>, 141<\/em>, 283\u2013285.
\n Masashi Mamada<\/span><\/strong>
\nDOI:10.1541\/ieejjournal.141.283<\/a><\/dd>\n<\/dl>\n
\n
[2]<\/dt>\n
\u6709\u6a5f\u534a\u5c0e\u4f53\u30ec\u30fc\u30b6\u30fc\u5206\u5b50\u306e\u8010\u4e45\u7279\u6027\u306e\u5411\u4e0a
\nVacuum and Surface Science<\/em>, 2021<\/strong>, 64<\/em>, 4\u20139.
\nChihaya Adachi, Masashi Mamada<\/span><\/strong>, Toshinori Matsushima
\nDOI:10.1380\/vss.64.4<\/a><\/dd>\n<\/dl>\n
\n
[1]<\/dt>\n
Polycyclic Arenes and Heteroarenes: Synthesis, Properties, and Applications
\nChapter 11, pp. 277\u2013308. Masashi Mamada<\/span><\/strong> and Yoshiro Yamashita, (2015) Wiley
\nDOI:10.1002\/9783527689545<\/a><\/dd>\n<\/dl>\n

\u7279\u8a31<\/h4>\n
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[8]<\/dt>\n
\u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u4e2d\u91ce\u8c37\u4e00\u3001\u5b89\u9054\u5343\u6ce2\u77e2\u3001\u30e4\u30f3\u30e6\u30bd\u30af
\n\u300c\u6709\u6a5f\u767a\u5149\u7d20\u5b50\u3001\u305d\u308c\u306b\u7528\u3044\u3089\u308c\u308b\u767a\u5149\u6750\u6599\u304a\u3088\u3073\u9045\u5ef6\u86cd\u5149\u4f53\u300d
\nPCT\/JP2017\/045788<\/dd>\n
[7]<\/dt>\n
\u6642\u4efb\u9759\u58eb\u3001\u718a\u6728\u5927\u4ecb\u3001 \u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u798f\u7530\u61b2\u4e8c\u90ce\u3001\u7530\u4e2d\u5eb7\u88d5\u3001\u5cf6\u79c0\u597d\u3001\u7c73\u7530\u5eb7\u6d0b\u3001\u57a3\u7530\u4e00\u6210\u3001\u5c0f\u4fe3\u6d0b\u6cbb\u3001\u5c71\u7530\u5948\u6d25\u5b50\u3001\u672c\u9593\u8cb4\u5fd7\u3001\u753a\u7530\u5229\u4e00\u3001\u85e4\u7530\u967d\u5e2b
\n\u300c\u30d9\u30f3\u30be\u30d3\u30b9\uff08\u30c1\u30a2\u30b8\u30a2\u30be\u30fc\u30eb\uff09\u8a98\u5c0e\u4f53\u3001\u304a\u3088\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u30c7\u30d0\u30a4\u30b9\u300d
\n\u7279\u9858\uff1aPCT\/JP2014\/072839<\/dd>\n
[6]<\/dt>\n
\u6642\u4efb\u9759\u58eb\u3001\u718a\u6728\u5927\u4ecb\u3001 \u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u7530\u4e2d\u5eb7\u88d5\u3001\u5cf6\u79c0\u597d\u3001\u7c73\u7530\u5eb7\u6d0b\u3001\u57a3\u7530\u4e00\u6210\u3001\u5c0f\u4fe3\u6d0b\u6cbb\u3001\u672c\u9593\u8cb4\u5fd7\u3001\u753a\u7530\u5229\u4e00
\n\u300c\u30d9\u30f3\u30be\u30d3\u30b9\uff08\u30c1\u30a2\u30b8\u30a2\u30be\u30fc\u30eb\uff09\u8a98\u5c0e\u4f53\u3001\u304a\u3088\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u30c7\u30d0\u30a4\u30b9\u300d
\n\u7279\u9858\uff1a2014-164975<\/dd>\n
[5]<\/dt>\n
\u6642\u4efb\u9759\u58eb\u3001\u718a\u6728\u5927\u4ecb\u3001 \u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u7530\u4e2d\u5eb7\u88d5\u3001\u5cf6\u79c0\u597d\u3001\u7c73\u7530\u5eb7\u6d0b\u3001\u57a3\u7530\u4e00\u6210\u3001\u5c0f\u4fe3\u6d0b\u6cbb\u3001\u753a\u7530\u5229\u4e00
\n\u300c\u30d9\u30f3\u30be\u30d3\u30b9\uff08\u30c1\u30a2\u30b8\u30a2\u30be\u30fc\u30eb\uff09\u8a98\u5c0e\u4f53\u3001\u304a\u3088\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u30c7\u30d0\u30a4\u30b9\u300d
\n\u7279\u9858\uff1a2014-174786<\/dd>\n
[4]<\/dt>\n
\u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u6642\u4efb\u9759\u58eb\u3001\u7247\u6850\u6d0b\u53f2\u3001\u5742\u4e0a\u77e5
\n\u300c\u30c6\u30c8\u30e9\u30bb\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u305d\u306e\u5408\u6210\u65b9\u6cd5\u4e26\u3073\u306b\u305d\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u30c7\u30d0\u30a4\u30b9\u300d
\n\u7279\u9858\uff1a2014-077476<\/dd>\n
[3]<\/dt>\n
\u6642\u4efb\u9759\u58eb\u3001\u718a\u6728\u5927\u4ecb\u3001 \u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u7530\u4e2d\u5eb7\u88d5\u3001\u5cf6\u79c0\u597d\u3001\u7c73\u7530\u5eb7\u6d0b\u3001\u85e4\u7530\u967d\u5e2b\u3001\u57a3\u7530\u4e00\u6210\u3001\u5c0f\u4fe3\u6d0b\u6cbb\u3001\u5c71\u7530\u5948\u6d25\u5b50\u3001\u672c\u9593\u8cb4\u5fd7\u3001\u753a\u7530\u5229\u4e00
\n\u300c\u30d9\u30f3\u30be\u30d3\u30b9\uff08\u30c1\u30a2\u30b8\u30a2\u30be\u30fc\u30eb\uff09\u8a98\u5c0e\u4f53\u3001\u305d\u308c\u3092\u542b\u3080\u30a4\u30f3\u30af\u3001\u304a\u3088\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u30c7\u30d0\u30a4\u30b9\u300d
\n\u7279\u9858\uff1a2014-026969<\/dd>\n
[2]<\/dt>\n
\u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u6642\u4efb\u9759\u58eb\u3001\u7247\u6850\u6d0b\u53f2\u3001\u718a\u6728\u5927\u4ecb\u3001\u6e21\u8fba\u7fd4\u4e00
\n\u300c\u30c6\u30c8\u30e9\u30a2\u30df\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u305d\u306e\u5408\u6210\u65b9\u6cd5\u4e26\u3073\u306b\u305d\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u30c7\u30d0\u30a4\u30b9\u300d
\n\u7279\u9858\uff1a2014-027138<\/dd>\n
[1]<\/dt>\n
\u6642\u4efb\u9759\u58eb\u3001\u718a\u6728\u5927\u4ecb\u3001 \u5118\u7530\u6b63\u53f2<\/span><\/strong>\u3001\u7530\u4e2d\u5eb7\u88d5\u3001\u5cf6\u79c0\u597d\u3001\u7c73\u7530\u5eb7\u6d0b\u3001\u57a3\u7530\u4e00\u6210\u3001\u5c0f\u4fe3\u6d0b\u6cbb\u3001\u5c71\u7530\u5948\u6d25\u5b50\u3001\u672c\u9593\u8cb4\u5fd7\u3001\u753a\u7530\u5229\u4e00
\n\u300c\u30d9\u30f3\u30be\u30d3\u30b9\uff08\u30c1\u30a2\u30b8\u30a2\u30be\u30fc\u30eb\uff09\u8a98\u5c0e\u4f53\u3001\u304a\u3088\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u30c7\u30d0\u30a4\u30b9\u300d
\n\u7279\u9858\uff1a2013-196221<\/dd>\n<\/dl>\n

\u56fd\u969b\u4f1a\u8b70\u767a\u8868<\/h4>\n
\n
[6]<\/dt>\n
(Invited) Synthesis, Aromaticity and Application to OFET and OLED of Peri-Pentacenopentacene
\n M. Mamada<\/span><\/strong>, Tanguy Jousselin-Oba, Karen Wright, J\u00e9rome Marrot, Chihaya Adachi, Abderrahim Yassar, Michel Frigoli
\n231st ECS Meeting, 2022, Vancouver.<\/dd>\n
[5]<\/dt>\n
(Invited) Development of highly emissive laser dyes for organic semiconductor laser diodes
\n M. Mamada<\/span><\/strong>, Chihaya Adachi
\nThe 13th Asian Conference on Organic Electronics (A-COE) 2021, Online.<\/dd>\n
[4]<\/dt>\n
(Invited) Singlet Biradical Compounds: Development and Application to Organic Electronic Devices
\n M. Mamada<\/span><\/strong>, Tanguy Jousselin-Oba, Chihaya Adachi, Michel Frigoli
\nAsian International Symposium \u2013 Organic Crystals, Chiba, Japan.<\/dd>\n
[3]<\/dt>\n
(Invited) A novel molecular design strategy for thermally activated delayed fluorescence materials
\n M. Mamada<\/span><\/strong>
\nFrance-Japan Workshop on Optoelectronics & Photonics 2018, Paris, France.<\/dd>\n
[2]<\/dt>\n
(Invited) High efficiency thermally activated delayed fluorescence through an excited-state intramolecular proton transfer
\n M. Mamada<\/span><\/strong>, K. Inada, T. Komino, W. J. Potscavage, H. Nakanotani, C. Adachi
\nSPIE Organic Light Emitting Materials and Devices XXI 2017, San Diego, USA.<\/dd>\n
[1]<\/dt>\n
(Invited) Isomer Effects on Semiconducting Properties in organic transistors
\n M. Mamada<\/span><\/strong>, S. Tokito
\nThe 5th Asian Conference on Organic Electronics (A-COE) 2013, POSTECH, Pohang, Korea.<\/dd>\n
<\/dd>\n<\/dl>\n","protected":false},"excerpt":{"rendered":"

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