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Deuterium isotope effect on the solid-state thermal isomerization of photo-coloured cis-keto species of N-salicylideneaniline.

Chemical communications (Cambridge, England)

Amimoto K, Kanatomi H, Nagakari A, Fukuda H, Koyama H, Kawato T.
PMID: 12739653
Chem Commun (Camb). 2003 Apr 07;(7):870-1. doi: 10.1039/b300830d.

Deuterium isotope kinetic effect in the solid state was observed by using thermal fading reaction of photo-coloured species derived from N-salicylideneaniline deuterohydroxyl derivative; thus, the existence of a cis-keto form in the photo-coloured Schiff base crystals was suggested experimentally...

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Amimoto K, Kanatomi H, Nagakari A, et al. Deuterium isotope effect on the solid-state thermal isomerization of photo-coloured cis-keto species of N-salicylideneaniline. Chem Commun (Camb). 2003;(7):870-1doi: 10.1039/b300830d.
Amimoto, K., Kanatomi, H., Nagakari, A., Fukuda, H., Koyama, H., & Kawato, T. (2003). Deuterium isotope effect on the solid-state thermal isomerization of photo-coloured cis-keto species of N-salicylideneaniline. Chemical communications (Cambridge, England), (7), 870-1. https://doi.org/10.1039/b300830d
Amimoto, Kiichi, et al. "Deuterium isotope effect on the solid-state thermal isomerization of photo-coloured cis-keto species of N-salicylideneaniline." Chemical communications (Cambridge, England) vol. ,7 (2003): 870-1. doi: https://doi.org/10.1039/b300830d
Amimoto K, Kanatomi H, Nagakari A, Fukuda H, Koyama H, Kawato T. Deuterium isotope effect on the solid-state thermal isomerization of photo-coloured cis-keto species of N-salicylideneaniline. Chem Commun (Camb). 2003 Apr 07;(7):870-1. doi: 10.1039/b300830d. PMID: 12739653.
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Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals.

Organic & biomolecular chemistry

Fukuda H, Amimoto K, Koyama H, Kawato T.
PMID: 12926290
Org Biomol Chem. 2003 May 07;1(9):1578-83. doi: 10.1039/b212295b.

N-(3,5-Dihalosalicylidene)-2,6-dialkylaniline derivatives were prepared and their structure and photochromic properties were investigated. From the X-ray crystallography, it was revealed that steric repulsion between the azomethine hydrogen atom and the alkyl groups at the 2,6-positions of the aniline ring lead...

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Fukuda H, Amimoto K, Koyama H, et al. Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals. Org Biomol Chem. 2003;1(9):1578-83doi: 10.1039/b212295b.
Fukuda, H., Amimoto, K., Koyama, H., & Kawato, T. (2003). Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals. Organic & biomolecular chemistry, 1(9), 1578-83. https://doi.org/10.1039/b212295b
Fukuda, Hisatane, et al. "Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals." Organic & biomolecular chemistry vol. 1,9 (2003): 1578-83. doi: https://doi.org/10.1039/b212295b
Fukuda H, Amimoto K, Koyama H, Kawato T. Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals. Org Biomol Chem. 2003 May 07;1(9):1578-83. doi: 10.1039/b212295b. PMID: 12926290.
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Bent-crystal monochromators for high-energy synchrotron radiation.

Journal of synchrotron radiation

Yamaoka H, Mochizuki T, Sakurai Y, Kawata H.
PMID: 15263624
J Synchrotron Radiat. 1998 May 01;5:699-701. doi: 10.1107/S0909049597018645. Epub 1998 May 01.

Two kinds of monochromators covering the energy ranges 100-150 keV and approximately 300 keV have been designed for inelastic (Compton) scattering experiments at the elliptical multipole wiggler beamline, BL08W, of SPring-8. Finite-element analyses using ANSYS for bent crystals indicate...

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Yamaoka H, Mochizuki T, Sakurai Y, et al. Bent-crystal monochromators for high-energy synchrotron radiation. J Synchrotron Radiat. 1998;5:699-701doi: 10.1107/S0909049597018645.
Yamaoka, H., Mochizuki, T., Sakurai, Y., & Kawata, H. (1998). Bent-crystal monochromators for high-energy synchrotron radiation. Journal of synchrotron radiation, 5699-701. https://doi.org/10.1107/S0909049597018645
Yamaoka, H, et al. "Bent-crystal monochromators for high-energy synchrotron radiation." Journal of synchrotron radiation vol. 5 (1998): 699-701. doi: https://doi.org/10.1107/S0909049597018645
Yamaoka H, Mochizuki T, Sakurai Y, Kawata H. Bent-crystal monochromators for high-energy synchrotron radiation. J Synchrotron Radiat. 1998 May 01;5:699-701. doi: 10.1107/S0909049597018645. Epub 1998 May 01. PMID: 15263624.
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Synthesis and photophysical properties of ferrocene-oligothiophene-fullerene triads.

The Journal of organic chemistry

Kanato H, Takimiya K, Otsubo T, Aso Y, Nakamura T, Araki Y, Ito O.
PMID: 15471467
J Org Chem. 2004 Oct 15;69(21):7183-9. doi: 10.1021/jo049137o.

To promote photoinduced charge separation previously observed for the oligothiophene-fullerene dyads (nT-C60), we have designed an additional attachment with a strongly electron-donating ferrocene at the unsubstituted terminal site of the oligothiophene and synthesized two types of the ferrocene-oligothiophene-fullerene triads,...

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Kanato H, Takimiya K, Otsubo T, et al. Synthesis and photophysical properties of ferrocene-oligothiophene-fullerene triads. J Org Chem. 2004;69(21):7183-9doi: 10.1021/jo049137o.
Kanato, H., Takimiya, K., Otsubo, T., Aso, Y., Nakamura, T., Araki, Y., & Ito, O. (2004). Synthesis and photophysical properties of ferrocene-oligothiophene-fullerene triads. The Journal of organic chemistry, 69(21), 7183-9. https://doi.org/10.1021/jo049137o
Kanato, Hiroki, et al. "Synthesis and photophysical properties of ferrocene-oligothiophene-fullerene triads." The Journal of organic chemistry vol. 69,21 (2004): 7183-9. doi: https://doi.org/10.1021/jo049137o
Kanato H, Takimiya K, Otsubo T, Aso Y, Nakamura T, Araki Y, Ito O. Synthesis and photophysical properties of ferrocene-oligothiophene-fullerene triads. J Org Chem. 2004 Oct 15;69(21):7183-9. doi: 10.1021/jo049137o. PMID: 15471467.
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Voltammetric study of interfacial electron transfer between bis(cyclopentadienyl)iron in organic solvents and hexacyanoferrate in water.

Analytical sciences : the international journal of the Japan Society for Analytical Chemistry

Tatsumi H, Katano H.
PMID: 15566159
Anal Sci. 2004 Nov;20(11):1613-5. doi: 10.2116/analsci.20.1613.

The electron-transfer reaction between bis(cyclopentadienyl)iron(II) ([Fe(II)(C5H5)2]) in nitrobenzene and a hexacyanoferrate redox couple ([Fe(II/III)(CN)6](4-/3-)) in water at the nitrobenzene / water interface was studied using normal pulse voltammetry. The voltammetric results indicate that the electron-transfer reaction takes place by...

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Tatsumi H, Katano H. Voltammetric study of interfacial electron transfer between bis(cyclopentadienyl)iron in organic solvents and hexacyanoferrate in water. Anal Sci. 2004;20(11):1613-5doi: 10.2116/analsci.20.1613.
Tatsumi, H., & Katano, H. (2004). Voltammetric study of interfacial electron transfer between bis(cyclopentadienyl)iron in organic solvents and hexacyanoferrate in water. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 20(11), 1613-5. https://doi.org/10.2116/analsci.20.1613
Tatsumi, Hirosuke, and Katano, Hajime. "Voltammetric study of interfacial electron transfer between bis(cyclopentadienyl)iron in organic solvents and hexacyanoferrate in water." Analytical sciences : the international journal of the Japan Society for Analytical Chemistry vol. 20,11 (2004): 1613-5. doi: https://doi.org/10.2116/analsci.20.1613
Tatsumi H, Katano H. Voltammetric study of interfacial electron transfer between bis(cyclopentadienyl)iron in organic solvents and hexacyanoferrate in water. Anal Sci. 2004 Nov;20(11):1613-5. doi: 10.2116/analsci.20.1613. PMID: 15566159.
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Structure and rheology of a self-standing nanoemulsion.

Langmuir : the ACS journal of surfaces and colloids

Kawada H, Kume T, Matsunaga T, Iwai H, Sano T, Shibayama M.
PMID: 20141204
Langmuir. 2010 Feb 16;26(4):2430-7. doi: 10.1021/la902905b.

A stable nanoemulsion consisting of nanometer-sized oil droplets in water having a self-standing capability was prepared by high-pressure emulsification. The nanoemulsion does not flow and has a yield stress. This nonfluidity is ascribed to the crystal-like lattice structure of...

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Kawada H, Kume T, Matsunaga T, et al. Structure and rheology of a self-standing nanoemulsion. Langmuir. 2010;26(4):2430-7doi: 10.1021/la902905b.
Kawada, H., Kume, T., Matsunaga, T., Iwai, H., Sano, T., & Shibayama, M. (2010). Structure and rheology of a self-standing nanoemulsion. Langmuir : the ACS journal of surfaces and colloids, 26(4), 2430-7. https://doi.org/10.1021/la902905b
Kawada, Hiromitsu, et al. "Structure and rheology of a self-standing nanoemulsion." Langmuir : the ACS journal of surfaces and colloids vol. 26,4 (2010): 2430-7. doi: https://doi.org/10.1021/la902905b
Kawada H, Kume T, Matsunaga T, Iwai H, Sano T, Shibayama M. Structure and rheology of a self-standing nanoemulsion. Langmuir. 2010 Feb 16;26(4):2430-7. doi: 10.1021/la902905b. PMID: 20141204.
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QUANTITATIVE MODELING OF SPATIO-TEMPORAL DYNAMICS OF INFERIOR OLIVE NEURONS WITH A SIMPLE CONDUCTANCE-BASED MODEL.

International journal of bifurcation and chaos in applied sciences and engineering

Katori Y, Lang EJ, Onizuka M, Kawato M, Aihara K.
PMID: 21637736
Int J Bifurcat Chaos. 2010 Mar;20(3):583-603. doi: 10.1142/S0218127410025909.

Inferior olive (IO) neurons project to the cerebellum and contribute to motor control. They can show intriguing spatio-temporal dynamics with rhythmic and synchronized spiking. IO neurons are connected to their neighbors via gap junctions to form an electrically coupled...

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Katori Y, Lang EJ, Onizuka M, et al. QUANTITATIVE MODELING OF SPATIO-TEMPORAL DYNAMICS OF INFERIOR OLIVE NEURONS WITH A SIMPLE CONDUCTANCE-BASED MODEL. Int J Bifurcat Chaos. 2010;20(3):583-603doi: 10.1142/S0218127410025909.
Katori, Y., Lang, E. J., Onizuka, M., Kawato, M., & Aihara, K. (2010). QUANTITATIVE MODELING OF SPATIO-TEMPORAL DYNAMICS OF INFERIOR OLIVE NEURONS WITH A SIMPLE CONDUCTANCE-BASED MODEL. International journal of bifurcation and chaos in applied sciences and engineering, 20(3), 583-603. https://doi.org/10.1142/S0218127410025909
Katori, Yuichi, et al. "QUANTITATIVE MODELING OF SPATIO-TEMPORAL DYNAMICS OF INFERIOR OLIVE NEURONS WITH A SIMPLE CONDUCTANCE-BASED MODEL." International journal of bifurcation and chaos in applied sciences and engineering vol. 20,3 (2010): 583-603. doi: https://doi.org/10.1142/S0218127410025909
Katori Y, Lang EJ, Onizuka M, Kawato M, Aihara K. QUANTITATIVE MODELING OF SPATIO-TEMPORAL DYNAMICS OF INFERIOR OLIVE NEURONS WITH A SIMPLE CONDUCTANCE-BASED MODEL. Int J Bifurcat Chaos. 2010 Mar;20(3):583-603. doi: 10.1142/S0218127410025909. PMID: 21637736; PMCID: PMC3104735.
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Proteomic analysis of proteins expressing in regions of rat brain by a combination of SDS-PAGE with nano-liquid chromatography-quadrupole-time of flight tandem mass spectrometry.

Proteome science

Katagiri T, Hatano N, Aihara M, Kawano H, Okamoto M, Liu Y, Izumi T, Maekawa T, Nakamura S, Ishihara T, Shirai M, Mizukami Y.
PMID: 20659346
Proteome Sci. 2010 Jul 27;8:41. doi: 10.1186/1477-5956-8-41.

BACKGROUND: Most biological functions controlled by the brain and their related disorders are closely associated with activation in specific regions of the brain. Neuroproteomics has been applied to the analysis of whole brain, and the general pattern of protein...

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Katagiri T, Hatano N, Aihara M, et al. Proteomic analysis of proteins expressing in regions of rat brain by a combination of SDS-PAGE with nano-liquid chromatography-quadrupole-time of flight tandem mass spectrometry. Proteome Sci. 2010;8:41doi: 10.1186/1477-5956-8-41.
Katagiri, T., Hatano, N., Aihara, M., Kawano, H., Okamoto, M., Liu, Y., Izumi, T., Maekawa, T., Nakamura, S., Ishihara, T., Shirai, M., & Mizukami, Y. (2010). Proteomic analysis of proteins expressing in regions of rat brain by a combination of SDS-PAGE with nano-liquid chromatography-quadrupole-time of flight tandem mass spectrometry. Proteome science, 841. https://doi.org/10.1186/1477-5956-8-41
Katagiri, Tomoki, et al. "Proteomic analysis of proteins expressing in regions of rat brain by a combination of SDS-PAGE with nano-liquid chromatography-quadrupole-time of flight tandem mass spectrometry." Proteome science vol. 8 (2010): 41. doi: https://doi.org/10.1186/1477-5956-8-41
Katagiri T, Hatano N, Aihara M, Kawano H, Okamoto M, Liu Y, Izumi T, Maekawa T, Nakamura S, Ishihara T, Shirai M, Mizukami Y. Proteomic analysis of proteins expressing in regions of rat brain by a combination of SDS-PAGE with nano-liquid chromatography-quadrupole-time of flight tandem mass spectrometry. Proteome Sci. 2010 Jul 27;8:41. doi: 10.1186/1477-5956-8-41. PMID: 20659346; PMCID: PMC2918549.
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Measurement of two-photon excitation spectrum used to photoconvert a fluorescent protein (Kaede) by nonlinear Fourier-transform spectroscopy.

Biomedical optics express

Isobe K, Hashimoto H, Suda A, Kannari F, Kawano H, Mizuno H, Miyawaki A, Midorikawa K.
PMID: 21258500
Biomed Opt Express. 2010 Aug 23;1(2):687-693. doi: 10.1364/BOE.1.000687.

We demonstrate the measurement of two-photon excitation (TPE) spectra, used not only for fluorescence but also for photoconversion in green-to-red photoconvertible Kaede, using nonlinear Fourier-transform spectroscopy. It was found that in unphotoconverted Kaede, the TPE spectrum for photoconversion is...

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Isobe K, Hashimoto H, Suda A, et al. Measurement of two-photon excitation spectrum used to photoconvert a fluorescent protein (Kaede) by nonlinear Fourier-transform spectroscopy. Biomed Opt Express. 2010;1(2):687-693doi: 10.1364/BOE.1.000687.
Isobe, K., Hashimoto, H., Suda, A., Kannari, F., Kawano, H., Mizuno, H., Miyawaki, A., & Midorikawa, K. (2010). Measurement of two-photon excitation spectrum used to photoconvert a fluorescent protein (Kaede) by nonlinear Fourier-transform spectroscopy. Biomedical optics express, 1(2), 687-693. https://doi.org/10.1364/BOE.1.000687
Isobe, Keisuke, et al. "Measurement of two-photon excitation spectrum used to photoconvert a fluorescent protein (Kaede) by nonlinear Fourier-transform spectroscopy." Biomedical optics express vol. 1,2 (2010): 687-693. doi: https://doi.org/10.1364/BOE.1.000687
Isobe K, Hashimoto H, Suda A, Kannari F, Kawano H, Mizuno H, Miyawaki A, Midorikawa K. Measurement of two-photon excitation spectrum used to photoconvert a fluorescent protein (Kaede) by nonlinear Fourier-transform spectroscopy. Biomed Opt Express. 2010 Aug 23;1(2):687-693. doi: 10.1364/BOE.1.000687. PMID: 21258500; PMCID: PMC3017996.
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Marked alteration of c-fos and c-jun but not hsp70 messenger RNA expression in rat brain after cold-induced trauma: An in situ hybridization study.

Restorative neurology and neuroscience

Katano H, Masago A, Yamada K.
PMID: 21551539
Restor Neurol Neurosci. 1997 Jan 01;11(3):153-60. doi: 10.3233/RNN-1997-11305.

Immediate early gene (IEG) mRNA induction by cryogenic injury was examined using an in situ hybridization approach and the results compared with the heat shock protein mRNA expression. Hybridization signals for c-fos and c-jun mRNA were found after 30...

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Katano H, Masago A, Yamada K. Marked alteration of c-fos and c-jun but not hsp70 messenger RNA expression in rat brain after cold-induced trauma: An in situ hybridization study. Restor Neurol Neurosci. 1997;11(3):153-60doi: 10.3233/RNN-1997-11305.
Katano, H., Masago, A., & Yamada, K. (1997). Marked alteration of c-fos and c-jun but not hsp70 messenger RNA expression in rat brain after cold-induced trauma: An in situ hybridization study. Restorative neurology and neuroscience, 11(3), 153-60. https://doi.org/10.3233/RNN-1997-11305
Katano, H, et al. "Marked alteration of c-fos and c-jun but not hsp70 messenger RNA expression in rat brain after cold-induced trauma: An in situ hybridization study." Restorative neurology and neuroscience vol. 11,3 (1997): 153-60. doi: https://doi.org/10.3233/RNN-1997-11305
Katano H, Masago A, Yamada K. Marked alteration of c-fos and c-jun but not hsp70 messenger RNA expression in rat brain after cold-induced trauma: An in situ hybridization study. Restor Neurol Neurosci. 1997 Jan 01;11(3):153-60. doi: 10.3233/RNN-1997-11305. PMID: 21551539.
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Correlation between severity of rheumatoid arthritis and manner and extent of cervical lesion.

Modern rheumatology

Mitsuka T, Miura T, Ueyama K, Sannohe A, Katano H, Toh S.
PMID: 24387649
Mod Rheumatol. 2004 Sep;14(4):301-5. doi: 10.3109/s10165-004-0313-6.

Abstract To determine the proper management of treatment for rheumatoid cervical lesions, we investigated the clinical course of the cervical spine in rheumatoid arthritis (RA). The severity of RA was classified into three groups according to the disease subsets...

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Mitsuka T, Miura T, Ueyama K, et al. Correlation between severity of rheumatoid arthritis and manner and extent of cervical lesion. Mod Rheumatol. 2004;14(4):301-5doi: 10.3109/s10165-004-0313-6.
Mitsuka, T., Miura, T., Ueyama, K., Sannohe, A., Katano, H., & Toh, S. (2004). Correlation between severity of rheumatoid arthritis and manner and extent of cervical lesion. Modern rheumatology, 14(4), 301-5. https://doi.org/10.3109/s10165-004-0313-6
Mitsuka, Takeshi, et al. "Correlation between severity of rheumatoid arthritis and manner and extent of cervical lesion." Modern rheumatology vol. 14,4 (2004): 301-5. doi: https://doi.org/10.3109/s10165-004-0313-6
Mitsuka T, Miura T, Ueyama K, Sannohe A, Katano H, Toh S. Correlation between severity of rheumatoid arthritis and manner and extent of cervical lesion. Mod Rheumatol. 2004 Sep;14(4):301-5. doi: 10.3109/s10165-004-0313-6. PMID: 24387649.
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{2,7-Dieth-oxy-8-[(naphthalen-1-yl)carbon-yl]naph-thalen-1-yl}(naphthalen-1-yl)methanone.

Acta crystallographica. Section E, Structure reports online

Tsumuki T, Takeuchi R, Kawano H, Yonezawa N, Okamoto A.
PMID: 23634045
Acta Crystallogr Sect E Struct Rep Online. 2013 Mar 06;69:o495-6. doi: 10.1107/S1600536813005710. Print 2013 Apr 01.

In the title compound, C36H28O4, the 1-naphthoyl groups at the 1- and 8-positions of the central 2,7-dieth-oxy-naphthalene ring system are aligned almost anti-parallel and make a dihedral angle of 76.59 (4)°. The dihedral angles between the central 2,7-dieth-oxy-naphthalene ring...

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Tsumuki T, Takeuchi R, Kawano H, et al. {2,7-Dieth-oxy-8-[(naphthalen-1-yl)carbon-yl]naph-thalen-1-yl}(naphthalen-1-yl)methanone. Acta Crystallogr Sect E Struct Rep Online. 2013;69:o495-6doi: 10.1107/S1600536813005710.
Tsumuki, T., Takeuchi, R., Kawano, H., Yonezawa, N., & Okamoto, A. (2013). {2,7-Dieth-oxy-8-[(naphthalen-1-yl)carbon-yl]naph-thalen-1-yl}(naphthalen-1-yl)methanone. Acta crystallographica. Section E, Structure reports online, 69o495-6. https://doi.org/10.1107/S1600536813005710
Tsumuki, Takehiro, et al. "{2,7-Dieth-oxy-8-[(naphthalen-1-yl)carbon-yl]naph-thalen-1-yl}(naphthalen-1-yl)methanone." Acta crystallographica. Section E, Structure reports online vol. 69 (2013): o495-6. doi: https://doi.org/10.1107/S1600536813005710
Tsumuki T, Takeuchi R, Kawano H, Yonezawa N, Okamoto A. {2,7-Dieth-oxy-8-[(naphthalen-1-yl)carbon-yl]naph-thalen-1-yl}(naphthalen-1-yl)methanone. Acta Crystallogr Sect E Struct Rep Online. 2013 Mar 06;69:o495-6. doi: 10.1107/S1600536813005710. Print 2013 Apr 01. PMID: 23634045; PMCID: PMC3629527.
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