Year |
Citation |
Score |
2018 |
Yamauchi M, Miyamoto Y, Suzuki M, Yamada H, Masuo S. Photoconversion of 6,13-α-diketopentacene single crystals exhibiting light intensity-dependent morphological change. Physical Chemistry Chemical Physics : Pccp. PMID 30575827 DOI: 10.1039/C8Cp06594B |
0.313 |
|
2018 |
Mei P, Matsumoto A, Hayashi H, Suzuki M, Aratani N, Yamada H. 1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C60 Rsc Advances. 8: 20872-20876. DOI: 10.1039/C8Ra03601B |
0.334 |
|
2017 |
Yamashita M, Kawano K, Matsumoto A, Aratani N, Hayashi H, Suzuki M, Zhang L, Briseno AL, Yamada H. Dinaphthotetrathiafulvalene Bisimides: A New Member of the Family of pi-Extended TTF Stable p-Type Semiconductors. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28675573 DOI: 10.1002/Chem.201702657 |
0.325 |
|
2017 |
Lin X, Suzuki M, Gushiken M, Yamauchi M, Karatsu T, Kizaki T, Tani Y, Nakayama KI, Suzuki M, Yamada H, Kajitani T, Fukushima T, Kikkawa Y, Yagai S. High-fidelity self-assembly pathways for hydrogen-bonding molecular semiconductors. Scientific Reports. 7: 43098. PMID 28225029 DOI: 10.1038/Srep43098 |
0.334 |
|
2017 |
Matsumoto A, Suzuki M, Hayashi H, Kuzuhara D, Yuasa J, Kawai T, Aratani N, Yamada H. Studies on Pyrene and Perylene Derivatives upon Oxidation and Application to a Higher Analogue Bulletin of the Chemical Society of Japan. 90: 667-677. DOI: 10.1246/Bcsj.20160337 |
0.303 |
|
2016 |
Matsumoto A, Suzuki M, Hayashi H, Kuzuhara D, Yuasa J, Kawai T, Aratani N, Yamada H. Aromaticity Relocation in Perylene Derivatives upon Two-electron Oxidation to Form Anthracene and Phenanthrene. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27429200 DOI: 10.1002/Chem.201602188 |
0.329 |
|
2016 |
Suzuki M, Guo Z, Tahara K, Kotyk JF, Nguyen H, Gotoda J, Iritani K, Rubin Y, Tobe Y. Self-Assembled Dehydro[24]annulene Monolayers at the Liquid/Solid Interface: Towards On-Surface Synthesis of Tubular π-Conjugated Nanowires. Langmuir : the Acs Journal of Surfaces and Colloids. PMID 27183003 DOI: 10.1021/Acs.Langmuir.6B00744 |
0.568 |
|
2016 |
Suzuki M, Kotyk JF, Khan S, Rubin Y. Directing the Crystallization of Dehydro[24]annulenes into Supramolecular Nanotubular Scaffolds. Journal of the American Chemical Society. PMID 27088651 DOI: 10.1021/Jacs.6B01939 |
0.578 |
|
2016 |
Sezukuri K, Suzuki M, Hayashi H, Kuzuhara D, Aratani N, Yamada H. A laterally π-expanded fluorone dye as an efficient near infrared fluorophore. Chemical Communications (Cambridge, England). PMID 26935292 DOI: 10.1039/C6Cc00237D |
0.304 |
|
2015 |
Matsumoto A, Suzuki M, Kuzuhara D, Hayashi H, Aratani N, Yamada H. Tetrabenzoperipentacene: Stable Five-Electron Donating Ability and a Discrete Triple-Layered β-Graphite Form in the Solid State. Angewandte Chemie (International Ed. in English). 54: 8175-8. PMID 26013495 DOI: 10.1002/Anie.201502466 |
0.33 |
|
2014 |
Okabe T, Kuzuhara D, Suzuki M, Aratani N, Yamada H. Synthesis and electrochemical properties of porphycene-diketopyrrolopyrrole conjugates. Organic Letters. 16: 3508-11. PMID 24937408 DOI: 10.1021/Ol5014608 |
0.303 |
|
2011 |
Halim M, Kennedy RD, Suzuki M, Khan SI, Diaconescu PL, Rubin Y. Complexes of gold(I), silver(I), and copper(I) with pentaaryl[60]fullerides. Journal of the American Chemical Society. 133: 6841-51. PMID 21476501 DOI: 10.1021/Ja201297R |
0.558 |
|
2010 |
Suzuki M, Comito A, Khan SI, Rubin Y. Nanochannel array within a multilayered network of a planarized dehydro[24]annulene. Organic Letters. 12: 2346-9. PMID 20402478 DOI: 10.1021/Ol1006967 |
0.622 |
|
2003 |
Murata Y, Suzuki M, Rubin Y, Komatsu K. Structure of the Hydration Product of the C60-Di(2-pyridyl)-1,2,4,5-tetrazine Adduct Bulletin of the Chemical Society of Japan. 76: 1669-1672. DOI: 10.1246/Bcsj.76.1669 |
0.556 |
|
2001 |
Murata Y, Suzuki M, Komatsu K. Synthesis and electrochemical properties of novel dimeric fullerenes incorporated in a 2,3-diazabicyclo[2.2.2]oct-2-ene framework Chemical Communications. 2338-2339. PMID 12240064 DOI: 10.1039/B107922K |
0.308 |
|
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