يعرض 1 - 20 نتائج من 62 نتيجة بحث عن '"Transient absorption spectra"', وقت الاستعلام: 0.63s تنقيح النتائج
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    المصدر: Proceedings of the National Academy of Sciences of Belarus. Physics and Mathematics Series; Том 57, № 2 (2021); 224-231 ; Известия Национальной академии наук Беларуси. Серия физико-математических наук; Том 57, № 2 (2021); 224-231 ; 2524-2415 ; 1561-2430 ; 10.29235/1561-2430-2021-57-2

    وصف الملف: application/pdf

    Relation: https://vestifm.belnauka.by/jour/article/view/589/488; Uzhinov, B. M. Conformational effects in excited state intramolecular proton transfer of organic compounds / B. M. Uzhinov, M. N. Khimich // Russ. Chem. Rev. – 2011. – Vol. 80, № 6. – P. 553–578. https://doi.org/10.1070/rc2011v080n06abeh004144; Mapping GFP structure evolution during proton transfer with femtosecond Raman spectroscopy / C. Fang [et al.] // Nature. – 2009. – Vol. 462, № 7272. – P. 200–205. https://doi.org/10.1038/nature08527; The Proton-Transfer Laser. Gain Spectrum and Amplification of Spontaneous Emission of 3-Hydroxyflavone / P.Chou [et al.] // J. Phys. Chem. – 1984. – Vol. 88, № 20. – P. 4596–4599. https://doi.org/10.1021/j150664a032; Fluorescence Studies of Salicylic Acid Doped Poly (Vinyl Alcohol) Film as a Water/Humidity Sensor / H Mishra [et al.] // J. Phys. Chem. A. – 2004. – Vol. 108, № 12. – P. 2346–2352. https://doi.org/10.1021/jp0309365; Sobolewski, A. L. Reversible Molecular Switch Driven by Excited-State Hydrogen Transfer / A. L. Sobolewski // Phys. Chem. Chem. Phys. – 2008. – Vol. 10, № 9. – P. 1243–1247. https://doi.org/10.1039/b716075e; Control of the Reversibility of Excited-State Intramolecular Proton Transfer (ESIPT) Reaction: Host-Polarity Tuning White Organic Light Emitting Diode on a New Thiazolo[5,4-d]Thiazole ESIPT System / Z. Zhang [et al.] // Chem. Mater. – 2016. – Vol. 28, № 23. – P. 8815–8824. https://doi.org/10.1021/acs.chemmater.6b04707; Ultrafast excited state intramolecular proton transfer (ESIPT) mechanism for 2,6-bis(benzothiazolyl-2-yl)phenol: A theoretical investigation / D. Yang [et al.] // Chem. Phys. Lett. – 2020. – Vol. 744. – P. 137226. https://doi.org/10.1016/j.cplett.2020.137226; Excited-State Intramolecular Proton Transfer in the Kinetic-Control Regime / Z.-Y. Liu [et al.] // Phys. Chem. Chem. Phys. – 2020. – Vol. 22, № 39. – P. 22271–22278. https://doi.org/10.1039/d0cp03408h; Taylor, C. A. Excited-State Two-Proton Tautomerism in Hydrogen-Bonded N-Heterocyclic Base Pairs / C. A. Taylor, M. A. El-Bayoumi, M. Kasha // Proc. Natl. Acad. Sci. USA. – 1969. – Vol. 63, № 2. – P. 253–260. https://doi.org/10.1073/pnas.63.2.253; Takeuchi, S. The answer to concerted versus step-wise controversy for the double proton transfer mechanism of 7-azaindole dimer in solution / S. Takeuchi, T. Tahara // Proc. Natl. Acad. Sci. USA. – 2007. – Vol. 104, № 13. – P. 5285–5290. https://doi.org/10.1073/pnas.0610141104; Kwon, O.-H. Double Proton Transfer Dynamics of Model DNA Base Pairs in the Condensed Phase / O.-H. Kwon, A. H. Zewail // Proc. Natl. Acad. Sci. USA. – 2007. – Vol. 104, № 21. – P. 8703–8708. https://doi.org/10.1073/pnas.0702944104; Pivovarenko, V. G. 2,8-Bis[4-(diethylamino)phenyl]-3,7-dihydroxy-4H,6H-pyrano[3,2-g]chromene-4,6-dione? A New Liquid-Phase-Sensitive Fluorescent Probe Utilising Intramolecular One- or Two-Proton Transfer Phenomena / V. G. Pivovarenko, L. Jozwiak, J. Blazejowski // Eur. J. Org. Chem. – 2002. – Vol. 2020, № 23. – P. 3979–3985. https://doi.org/10.1002/1099-0690(200212)2002:233.0.co;2-5; Falkovskaia, E. Interplay between Intra- and Intermolecular Excited-State Single- and Double-Proton-Transfer Processes in the Biaxially Symmetric Molecule 3,7-Dihydroxy-4H,6H-pyrano[3,2-g]-chromene-4,6-dione / E. Falkovskaia, V. G. Pivovarenko, J. C. del Valle // J. Phys. Chem. A. – 2003.– Vol. 107, № 18. – P. 3316–3325. https://doi.org/10.1021/jp021791p; Photodynamics of intramolecular proton transfer in polar and nonpolar biflavonoid solutions / S. L. Bondarev [et al.] // Opt. Spectrosc. – 2012. – Vol. 113, № 4. – P. 401–410. https://doi.org/10.1134/s0030400x12070065; Solvent polarity effect on nonradiative decay rate of Thioflavin T / V. I. Stsiapura [et al.] // J. Phys. Chem. A. – 2016. – Vol. 120, № 28. – P. 5481–5496. https://doi.org/10.1021/acs.jpca.6b02577; https://vestifm.belnauka.by/jour/article/view/589

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    المساهمون: Universitat Politècnica de València. Departamento de Química - Departament de Química, Generalitat Valenciana, Ministerio de Economía y Competitividad

    Relation: Journal of Photochemistry and Photobiology B Biology; info:eu-repo/grantAgreement/MINECO//CTQ2015-71004-R/ES/NANOGELES MOLECULARES FOTOACTIVOS ORIENTADOS A LA SOLUCION DE RETOS BIOMEDICOS/; info:eu-repo/grantAgreement/MINECO//CTQ2016-78875-P/ES/CONTROL SUPRAMOLECULAR DE LA FOTORREACTIVIDAD EN MEDIOS MICROHETEROGENOS BASADOS EN AMINOACIDOS: GELES MOLECULARES Y PROTEINAS TRANSPORTADORAS COMO NANORREACTORES/; info:eu-repo/grantAgreement/GVA//PROMETEO%2F2017%2F075/ES/Reacciones fotoquímicas de biomoléculas/; https://doi.org/10.1016/j.jphotobiol.2019.111686; urn:issn:1011-1344; http://hdl.handle.net/10251/171324

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    المصدر: Proceedings of the National Academy of Sciences of Belarus. Physics and Mathematics Series; Том 56, № 4 (2020); 470–479 ; Известия Национальной академии наук Беларуси. Серия физико-математических наук; Том 56, № 4 (2020); 470–479 ; 2524-2415 ; 1561-2430 ; 10.29235/1561-2430-2020-56-4

    وصف الملف: application/pdf

    Relation: https://vestifm.belnauka.by/jour/article/view/555/461; Leznoff, C. C. Phthalocyanines: properties and applications / C. C. Leznoff, A. B. P. Lever. – Weinheim: VCH, 1996. – Vol. 4. – 536 p.; Hohnholz, D. Applications of phthalocyanines in organic light emitting devices / D. Hohnholz, S. Steinbrecherb, M. Hanack // J. Mol. Struct. – 2000. – Vol. 521, № 1/3. – P. 231–237. https://doi.org/10.1016/s0022-2860(99)00438-x; 4.2% efficient organic photovoltaic cells with low series resistances / J. Xue [et al.] // Appl. Phys. Lett. – 2004. – Vol. 84, № 16. – P. 3013–3015. https://doi.org/10.1063/1.1713036; Van Flassen, E. Explanation of the low oxigen sensitivity of thin film phthalocyanine gas sensors / E. Van Flassen, H. Kerp // Sens. Actuators B: Chemical. – 2003. – Vol. 88, № 3. – P. 329–333. https://doi.org/10.1016/s0925-4005(02)00379-9; Surface-enhanced non-linear Raman scattering at the single-molecule level / K. Kneipp [et al.] // Chem. Phys. – 1999. – Vol. 247, № 1. – P. 155–162. https://doi.org/10.1016/s0301-0104(99)00165-2; Optimization of nanoparticle size for plasmonic enhancement of fluorescence / O. Stranik [et al.] // Plasmonics. – 2007. – Vol. 2, № 1. – P. 15–22. https://doi.org/10.1007/s11468-006-9020-9; Замковец, А. Д. Влияние эффектов ближнего поля на спектральные свойства слоистых нанокомпозитов серебро-фталоцианин меди / А. Д. Замковец, А. Н. Понявина // Журн. приклад. спектроскопии. – 2012. – Т. 79, № 6. – C. 907–912.; Plasmon-Related Modification of Spectral Kinetic Properties of Copper Phthalocyanine Thin Films in the Presence of Silver Nanoparticles / O. V. Buganov [et al.] // J. App. Spectrosc. – 2014. – Vol. 81, № 1. – P. 92–96. https://doi.org/10.1007/s10812-014-9892-y; Charge transfer process determines ultrafast excited state deactivation of thioflavin T in low-viscosity solvents / V. I. Stsiapura [et al.] // J. Phys. Chem. A. – 2010. – Vol. 114, № 32. – P. 8345−8350. https://doi.org/10.1021/jp105186z; Sergeeva, N. N. Photochemical Transformations Involving Porphyrins and Phthalocyanines / N. N. Sergeeva, M. O. Senge // CRC Handbook of Organic Photochemistry and Photobiology. – 2012 – P. 831–879. https://doi.org/10.1201/b12252-35; Mack, J. Assignment of the optical spectra of metal phthalocyanines through spectral band deconvolution analysis and ZINDO calculations / J. Mack, M. J. Stillman // Coord. Chem. Rev. – 2001. – Vol. 219, № 221. – P. 993–1032. https://doi.org/10.1016/s0010-8545(01)00394-0; Влияние структуры молекул фталоцианинов меди на характер их упорядочения в тонких пленках, спектры фотолюминесценции и поглощения / В. Л. Берковиц [и др.] // Физика твердого тела. – 2007. – Т. 49, № 2. – С. 262–266.; Vincett, P. S. Phosphorescence and Fluorescence of Phthalocyanines / P. S. Vincett, E. M. Voigt, K. E. Rieckhoff // J. Chem. Phys. – 1971. –Vol. 55, № 8. – P. 4131–4140. https://doi.org/10.1063/1.1676714; https://vestifm.belnauka.by/jour/article/view/555

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    وصف الملف: application/pdf

    Relation: info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F87786%2F2012/PT; info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F78037%2F2011/PT; info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F97026%2F2013/PT; SFRH/BPD/108469/2015; PEst-C/QUI/UI0686/2013 (FCOMP-01-0124-FEDER-037302); POCI-01-0145-FEDER-016387; Grant agreement no. 284464, EC’s Seventh Framework Programme; Fernandes, S. S. M.; Castro, M. C. R.; Pereira, A. I.; Mendes, A.; Serpa, C.; Pina, J.; Justino, L. L. G.; Burrows, H. D.; Raposo, M. M. M.; ACS Omega, 2017, 2 (12), pp 9268–9279; http://hdl.handle.net/1822/50176

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