Masaki Hasegawa

ORCID: 0000-0002-8925-6031
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Research Areas
  • Crystallization and Solubility Studies
  • Synthesis and properties of polymers
  • X-ray Diffraction in Crystallography
  • Photopolymerization techniques and applications
  • Photochromic and Fluorescence Chemistry
  • Analytical Chemistry and Chromatography
  • Synthetic Organic Chemistry Methods
  • Advanced Polymer Synthesis and Characterization
  • Polydiacetylene-based materials and applications
  • Asymmetric Synthesis and Catalysis
  • Molecular spectroscopy and chirality
  • Photochemistry and Electron Transfer Studies
  • Chemical Synthesis and Reactions
  • Inorganic and Organometallic Chemistry
  • Radical Photochemical Reactions
  • Synthesis and Properties of Aromatic Compounds
  • Liquid Crystal Research Advancements
  • Synthesis and Biological Evaluation
  • Crystallography and molecular interactions
  • Chemical Synthesis and Analysis
  • Silicone and Siloxane Chemistry
  • Oxidative Organic Chemistry Reactions
  • Porphyrin and Phthalocyanine Chemistry
  • Chemistry and Chemical Engineering
  • Organic Chemistry Cycloaddition Reactions

Yokohama National University
2024

Toyota Central Research and Development Laboratories (Japan)
2018-2022

National Center for Geriatrics and Gerontology
2020

The University of Tokyo
1985-2019

Merck (Japan)
2012-2019

TDK (Japan)
2016

Toyota Motor Corporation (Switzerland)
2016

Nippon Dental University Hospital
2015

Nagoya Medical Center
2010

University of Aizu
2003-2009

Exposure of positive-type polyimide (PI) to linearly polarized deep UV (DUV) light (257nm) induced homogeneous alignment nematic liquid crystals. The state changed markedly at a particular energy the light. Measurement absorption spectrum and retardation change generated in PI films by irradiation showed that anisotropic was caused new mechanism, photodepolymerization main chains parallel electric field DUV light.We monodomain exposing direction perpendicular DUV, its condition suddenly...

10.2494/photopolymer.8.241 article EN Journal of Photopolymer Science and Technology 1995-01-01

10.1002/pol.1967.110050915 article EN Journal of Polymer Science Part B Polymer Letters 1967-09-01

Abstract Crystalline 2,5‐distyrylpyrazine (DSP) was found to polymerize into a linear high polymer with extremely crystallinity by the action of sunlight or ultraviolet light. Based on this discovery, photopolymerizability related diolefins having general formula, trans , ‐Ar′CHCHArCHCHAr′ surveyed. As result, 1,4‐bis[β‐pyridyl‐(2)‐vinyl]benzene (P2VB) in same way as DSP. The polymers polymerized, showed melting temperature (>330°C) and were soluble only strong acids. structure...

10.1002/pol.1969.150070227 article EN Journal of Polymer Science Part A-1 Polymer Chemistry 1969-02-01

Abstract A new preparative route to photocrosslinkable polymers in which the are produced directly from polymerization of vinyl monomers having groups has been investigated. The photosensitive resins thus have higher sensitivity and resolution than conventional resins. were synthesized esterification vinylphenols or β‐chloroethyl ether with cinnamic acid, β‐styrylacrylic their homologs, etherification hydroxychalcones. Homopolymerizations these copolymerizations other comonomers investigated...

10.1002/pol.1971.150090801 article EN Journal of Polymer Science Part A-1 Polymer Chemistry 1971-08-01

Abstract

10.1351/pac198658091179 article EN Pure and Applied Chemistry 1986-01-01

Abstract The polymerization mechanism of trans , ‐2,5‐distyrylpyrazine (DSP) has been investigated and some crystal changes along with the process have observed through polarizing microscope x‐ray diffraction pattern. Information obtained on active species, reaction type, other factors such as light intensity, temperature, or crystalline state. DSP occurs only in solid state by photoirradiation. Reduced viscosity increases gradually increase conversion sharply above 80% conversion....

10.1002/pol.1969.150070228 article EN Journal of Polymer Science Part A-1 Polymer Chemistry 1969-02-01

Abstract 2,5-Distyrylpyrazine(C20H16N2), which has photo-polymerizability in the crystalline state, crystallizes orthorhombic system with cell dimensions of a=20.638, b=9.599, and c=7.655 Å, including four molecules unit cell. The space group is Pbca. structure been determined by direct method refined block-diagonal-matrix least-squares using three-dimensional data. not planar; average plane pyrazine ring makes a dihedral angle 12.09° that benzene ring. are spaced c-translation forming an...

10.1246/bcsj.44.1262 article EN Bulletin of the Chemical Society of Japan 1971-05-01

Abstract The solid‐state photopolymerization of phenylene diacrylic acid (PDA) and its derivatives was studied as an application photodimerization cinnamic to corresponding bifunctional molecule which has two units in a single molecule. p ‐ m ‐PDA, their esters amides were prepared investigated with respect photopolymerizability. Many them have been found polymerize into linear high polymers the cyclobutane rings main chain on irradiation by ultraviolet or visible light. polymerization...

10.1002/pol.1969.150070826 article EN Journal of Polymer Science Part A-1 Polymer Chemistry 1969-08-01

Abstract Further work on the polymerization of 1,3‐cyclohexadiene by action Zieglertype catalysis and cationic initiation has been carried out polymers with an inherent viscosity 0.1–0.19 have obtained consistently. Dehydrogenation poly‐1,3‐cyclohexadiene halogenation followed pyrolysis given good conversion to a polyphenyl which some units are incompletely aromatized. This polymer very heat stability but is not useful for plastic purposes.

10.1002/pol.1963.100010623 article EN Journal of Polymer Science Part A General Papers 1963-06-01

EZ-Photoisomerization has been attained for several kinds of salts α,β-unsaturated carboxylic acids with amines. This photoreaction proven to be an effective method preparing (Z)-isomers from ammonium (E)-α,β-unsaturated carboxylates. The isomerizability is strikingly altered upon changing the group, which implies that crystal structure affected reactivity a considerable extent. However, cavity in found have less influence than expected on isomerizability. A further detailed study concerning...

10.1039/p29960000247 article EN Journal of the Chemical Society. Perkin transactions II 1996-01-01

Abstract (±)-1,2-Diphenylethylenediamine (DPEDA) was efficiently resolved by the fractional crystallization of its diastereomeric salts with optically active mandelic acid. 1H-NMR spectrum N-monoacylated DPEDA an derivatizing agent showed that thus obtained pure.

10.1246/bcsj.59.931 article EN Bulletin of the Chemical Society of Japan 1986-03-01

Abstract Changes in crystal structure during polymerization and oligomerization of 2,5‐distyrylpyrazine have been investigated by x‐ray crystallography. The polymer the oligomer as obtained are three‐dimensionally oriented, directions three axes resultant crystals coincide with those original crystal. space group products also agrees that monomer. It is concluded approximately duplicate molecular arrangement monomer mechanism discussed on basis structures.

10.1002/pol.1972.160100811 article EN Journal of Polymer Science Part A-2 Polymer Physics 1972-08-01

We fabricated sheets consisting of aligned electrospun polymer nanofibers embedded with semiconductor nanorods (NRs) and confirmed the production polarized fluorescence emission. Electrospun NRs were rolled around a drum to form sheet in which each nanofiber was parallel rotation direction. The thickness polarization ratio 1.5 μm 0.6, respectively. also examined how electrospinning parameters affected sheet.

10.1063/1.4907548 article EN Applied Physics Letters 2015-02-02

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDiastereoselective ring-opening aldol-type reaction of 2,2-dialkoxycyclopropanecarboxylic esters with carbonyl compounds. 1. Synthesis cis 3,4-substituted .gamma.-lactonesShigeru Shimada, Yukihiko Hashimoto, Atsushi Sudo, Masaki Hasegawa, and Kazuhiko SaigoCite this: J. Org. Chem. 1992, 57, 26, 7126–7133Publication Date (Print):December 1, 1992Publication History Published online1 May 2002Published inissue 1 December...

10.1021/jo00052a028 article EN The Journal of Organic Chemistry 1992-12-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSynthesis and selective molecular recognition of a macrotricyclic receptor having crown ether cyclophane subunits as binding sitesKazuhiko Saigo, Nobuhiro Kihara, Yukihiko Hashimoto, Ru Jang Lin, Hiroshi Fujimura, Yoshihiro Suzuki, Masaki HasegawaCite this: J. Am. Chem. Soc. 1990, 112, 3, 1144–1150Publication Date (Print):January 1, 1990Publication History Published online1 May 2002Published inissue 1 January...

10.1021/ja00159a039 article EN Journal of the American Chemical Society 1990-01-01

The photochemical behaviour of fifteen derivatives head-to-head coumarin dimers has been investigated. photocleavage the cyclobutane rings in these compounds solution occurs on irradiation with light wavelength 277 ± 10 nm to give two molecules via symmetric fission and/or 2,2′-dihydroxystilbene and fumaric (and maleic) acid asymmetric fission. direction photofissions is primarily affected by basic structure dimer derivative, proceeding exclusively retention ring when derivative a stable...

10.1039/p19830001083 article EN Journal of the Chemical Society. Perkin transactions I/Journal of the Chemical Society. Perkin transactions. I 1983-01-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTopochemical double photocyclodimerization of the 1,4-dicinnamoylbenzene crystalMasaki Hasegawa, Kazuhiko Saigo, Toru Mori, Hirofumi Uno, Masao Nohara, and Hachiro NakanishiCite this: J. Am. Chem. Soc. 1985, 107, 9, 2788–2793Publication Date (Print):May 1, 1985Publication History Published online1 May 2002Published inissue 1 1985https://pubs.acs.org/doi/10.1021/ja00295a035https://doi.org/10.1021/ja00295a035research-articleACS PublicationsRequest...

10.1021/ja00295a035 article EN Journal of the American Chemical Society 1985-05-01
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