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Hiroshi Nishihara

Researcher at Keio University

Publications -  677
Citations -  17201

Hiroshi Nishihara is an academic researcher from Keio University. The author has contributed to research in topics: Medicine & Terpyridine. The author has an hindex of 62, co-authored 616 publications receiving 14683 citations. Previous affiliations of Hiroshi Nishihara include Tokyo University of Science & Ochanomizu University.

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Heteroleptic [Bis(oxazoline)](dipyrrinato)zinc(II) Complexes: Bright and Circularly Polarized Luminescence from an Originally Achiral Dipyrrinato Ligand

TL;DR: Heteroleptic zinc(II) complexes synthesized using achiral dipyrrinato and chiral bis(oxazoline) ligands show bright fluorescence with quantum efficiencies of up to 0.70, and the luminescence is circularly polarized despite the achirality of the dipyrinato ligand.
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Dual emission caused by ring inversion isomerization of a 4-methyl-2-pyridyl-pyrimidine copper(I) complex.

TL;DR: A new convertible copper(I) complex using 2-pyridyl-4-methylpyrimidine and diphosphine as ligands exhibited mechanical bistability based on the inversion motion of the pyrimidine ring, leading to dual luminescence behavior.
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Redox-Assisted Ring Closing Reaction of the Photogenerated Cyclophanediene Form of Bis(ferrocenyl)dimethyldihydropyrene with Interferrocene Electronic Communication Switching

TL;DR: Reversible switching of electronic communication between the ferrocene (Fc) moieties by photoisomerization of the DHP moiety is exhibited and a novel ring closing reaction induced by oxidation of the Fc moieties is demonstrated.
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GPR68, a proton-sensing GPCR, mediates interaction of cancer-associated fibroblasts and cancer cells.

TL;DR: CAF‐expressed GPR68 is a mediator of low‐pH‐promoted regulation of the tumor microenvironments, in particular to PDAC cell‐CAF interaction and may be a novel therapeutic target for pancreatic and perhaps other types of cancers.
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Synthesis of Azo-Conjugated Metalladithiolenes and Their Photo- and Proton-Responsive Isomerization Reactions

TL;DR: It is indicated that the protonation is a common feature for the azo-conjugated metalladithiolenes, but trans-to-cis photoisomerization is strongly dependent on the electronic structure of the trans form or a steric effect in the cis form.