Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Wataru Setaka"'
Publikováno v:
Chemistry, Vol 3, Iss 1, Pp 39-44 (2021)
Molecular rotors have earned substantial popularity in recent times, owing to the unique dependence of its crystalline properties on the rotational dynamics of the rotor. We have recently reported the synthesis and crystal structure of a phenylene-br
Externí odkaz:
https://doaj.org/article/3bc9e381cf2642b2bfecdc6d3ca8c5f7
Publikováno v:
Organic & Biomolecular Chemistry; 9/14/2024, Vol. 22 Issue 34, p6950-6954, 5p
Autor:
Reina Yoshizawa, Yusuke Inagaki, Hiroyuki Momma, Eunsang Kwon, Kazuaki Ohara, Kentaro Yamaguchi, Wataru Setaka
Publikováno v:
New Journal of Chemistry. 47:5946-5952
Solid-state fluorescence was quenched by libration of a fluorophore in a dimethylfluorene-diyl bridged macrocage.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a123369fd7b14e6fa53e350707086b4
https://doi.org/10.1039/d2nj05873a
https://doi.org/10.1039/d2nj05873a
Publikováno v:
The Journal of Organic Chemistry. 87:12783-12790
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6973b80335864ed435372d1db1289d1b
https://doi.org/10.1021/acs.joc.2c01398
https://doi.org/10.1021/acs.joc.2c01398
Publikováno v:
The Journal of Organic Chemistry. 87:10869-10875
Phenylenediamine derivatives have been investigated as functional molecules because of their characteristic oxidation properties. In this study, phenylene-bridged diazacycloalkanes, that is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d99970e797d7ba875a302c8e8c44c3ae
https://doi.org/10.1021/acs.joc.2c01174
https://doi.org/10.1021/acs.joc.2c01174
Publikováno v:
Organic & Biomolecular Chemistry. 20:7092-7098
The chemistry of artificial molecular rotors has recently attracted considerable attention in the field of molecular machines. Phenyltriptycene could be used as a stepwise molecular rotor because it is composed of a phenyl rotor and a triptycene stat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36663822a84394b0a37bf16e1674bda1
https://doi.org/10.1039/d2ob01179d
https://doi.org/10.1039/d2ob01179d
Publikováno v:
Organic & Biomolecular Chemistry.
Ditriptycylmethanes are known as molecular bevel gears, because the two triptycyl groups act as wheels and display correlated rotation in solution. However, introduction of substituents on the methylene-junction for chemical...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b31c7ca4d8155f1dd1a2ce7abda0cae
https://doi.org/10.1039/d3ob00666b
https://doi.org/10.1039/d3ob00666b
Publikováno v:
Chemical Communications. 57:7838-7841
Facile and simultaneous synthesis of diphenyl-disilabicyclo[14.14.14]alkane in/out-isomers was achieved by using organosilicon chemistry. Although the formation of several in/out-isomers would be conceivable, only two diastereomers, i.e. the (traditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1045d82ab9e41d782db1ce7267765164
https://doi.org/10.1039/d1cc02933a
https://doi.org/10.1039/d1cc02933a
Publikováno v:
Organic & Biomolecular Chemistry. 19:6328-6333
Intramolecular charge transfer (ICT) fluorescence has been widely investigated and exploited in sensor molecules. However, steric effects on the ICT fluorescence properties have rarely been reported so far, although research in this area would promot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc683d7967b4c83b1d0896d2cf723b01
https://doi.org/10.1039/d1ob01050f
https://doi.org/10.1039/d1ob01050f
Publikováno v:
Chemistry Letters. 50:1397-1399
A facile and novel template synthesis of flexible disilamacrocyclic compounds via a ring-closing metathesis coupling was achieved. The structures of the macrocycles were determined by X-ray crystal...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1ae2871c0ae3c53d7729390d8bf8b9a
https://doi.org/10.1246/cl.210234
https://doi.org/10.1246/cl.210234