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Volumn 8, Issue 11, 2009, Pages 1603-1610

Temperature influence on deactivation paths and tautomeric equilibrium of some photochromic Schiff bases studied by time-resolved and stationary spectroscopy

Author keywords

[No Author keywords available]

Indexed keywords

SCHIFF BASE; TRIFLUOROETHANOL;

EID: 71049150527     PISSN: 1474905X     EISSN: 14749092     Source Type: Journal    
DOI: 10.1039/b9pp00040b     Document Type: Article
Times cited : (11)

References (32)
  • 1
    • 11844254512 scopus 로고    scopus 로고
    • Photochromism and thermochromism of Schiff bases in the solid state: Structural aspects
    • E. Hadjoudis I. M. Mavridis Photochromism and thermochromism of Schiff bases in the solid state: Structural aspects Chem. Soc. Rev. 2004 33 579
    • (2004) Chem. Soc. Rev. , vol.33 , pp. 579
    • Hadjoudis, E.1    Mavridis, I.M.2
  • 2
    • 25444439011 scopus 로고    scopus 로고
    • Design, synthesis, structural and nonlinear optical properties of photochromic crystals: Toward reversible molecular switches
    • M. Sliwa S. Letard I. Malfant M. Nierlich P. G. Lacroix T. Asahi H. Masuhara P. Yu K. Nakatani Design, Synthesis, Structural and Nonlinear Optical Properties of Photochromic Crystals: Toward Reversible Molecular Switches Chem. Mater. 2005 17 4727 4735
    • (2005) Chem. Mater. , vol.17 , pp. 4727-4735
    • Sliwa, M.1    Letard, S.2    Malfant, I.3    Nierlich, M.4    Lacroix, P.G.5    Asahi, T.6    Masuhara, H.7    Yu, P.8    Nakatani, K.9
  • 3
    • 0000527186 scopus 로고    scopus 로고
    • Special issue on photochromism: Memories and switches
    • M. Irie special issue on Photochromism: Memories and Switches Chem. Rev. 2000 100 1683
    • (2000) Chem. Rev. , vol.100 , pp. 1683
    • Irie, M.1
  • 4
    • 0142243465 scopus 로고
    • Photochromism of salicylidene aniline
    • R. V. Andes D. M. Manikowski Photochromism of salicylidene aniline Appl. Opt. 1968 7 1179
    • (1968) Appl. Opt. , vol.7 , pp. 1179
    • Andes, R.V.1    Manikowski, D.M.2
  • 5
    • 8144226447 scopus 로고    scopus 로고
    • An ultrafast excited state intramolecular proton transfer (ESPIT) and photochromism of salicylideneaniline (SA) and its ''double" analogue salicylaldehyde azine (SAA). A controversial case
    • M. Ziółek J. Kubicki A. Maciejewski R. Naskrcki A. Grabowska An ultrafast excited state intramolecular proton transfer (ESPIT) and photochromism of salicylideneaniline (SA) and its ''double" analogue salicylaldehyde azine (SAA). A controversial case Phys. Chem. Chem. Phys. 2004 6 4682 4689
    • (2004) Phys. Chem. Chem. Phys. , vol.6 , pp. 4682-4689
    • Ziółek, M.1    Kubicki, J.2    MacIejewski, A.3    Naskrcki, R.4    Grabowska, A.5
  • 6
    • 34547506930 scopus 로고    scopus 로고
    • Excited state intramolecular proton transfer in schiff bases. decay of the locally excited enol state observed by femtosecond resolved fluorescence
    • W. Rodríguez-Córdoba J. S. Zugazagoitia E. Collado-Fregoso J. Peon Excited State Intramolecular Proton Transfer in Schiff Bases. Decay of the Locally Excited Enol State Observed by Femtosecond Resolved Fluorescence J. Phys. Chem. A 2007 111 6241 6247
    • (2007) J. Phys. Chem. A , vol.111 , pp. 6241-6247
    • Rodríguez-Córdoba, W.1    Zugazagoitia, J.S.2    Collado-Fregoso, E.3    Peon, J.4
  • 7
    • 57449099511 scopus 로고    scopus 로고
    • Electronic-structure and quantum dynamical study of the photochromism of the aromatic Schiff base salicylideneaniline
    • J. M. Ortiz-Sánchez R. Gelabert M. Moreno J. M. Lluch Electronic-structure and quantum dynamical study of the photochromism of the aromatic Schiff base salicylideneaniline J. Chem. Phys. 2008 129 214308
    • (2008) J. Chem. Phys. , vol.129 , pp. 214308
    • Ortiz-Sánchez, J.M.1    Gelabert, R.2    Moreno, M.3    Lluch, J.M.4
  • 8
    • 0035849245 scopus 로고    scopus 로고
    • Wave-packet-assisted decomposition of femtosecond transient uv/vis absorption spectra: Application to excited-state intramolecular proton transfer in solution
    • N. P. Ernsting S. A. Kovalenko T. Senyushkina J. Saam V. Farztdinov Wave-Packet-Assisted Decomposition of Femtosecond Transient UV/vis Absorption Spectra: Application to Excited-State Intramolecular Proton Transfer in Solution J. Phys. Chem. A 2001 105 3443 3453
    • (2001) J. Phys. Chem. A , vol.105 , pp. 3443-3453
    • Ernsting, N.P.1    Kovalenko, S.A.2    Senyushkina, T.3    Saam, J.4    Farztdinov, V.5
  • 9
    • 0036970106 scopus 로고    scopus 로고
    • Femtosecond mid-infrared spectroscopy of condensed phase hydrogen-bonded systems as a probe of structural dynamics
    • M. Rini A. Kummrow J. Dreyer E. T. J. Nibbering T. Elsaesser Femtosecond mid-infrared spectroscopy of condensed phase hydrogen-bonded systems as a probe of structural dynamics Faraday Discuss. 2003 122 27 40
    • (2003) Faraday Discuss. , vol.122 , pp. 27-40
    • Rini, M.1    Kummrow, A.2    Dreyer, J.3    Nibbering, E.T.J.4    Elsaesser, T.5
  • 10
    • 0345800705 scopus 로고    scopus 로고
    • Microscopic mechanism of ultrafast excited-state intramolecular proton transfer: A 30-fs study of 2-(2′-hydroxyphenyl)benzothiazole
    • S. Lochbrunner A. J. Wurzer E. Riedle Microscopic mechanism of ultrafast excited-state intramolecular proton transfer: A 30-fs study of 2-(2′-hydroxyphenyl)benzothiazole J. Phys. Chem. A 2003 107 10580 10590
    • (2003) J. Phys. Chem. A , vol.107 , pp. 10580-10590
    • Lochbrunner, S.1    Wurzer, A.J.2    Riedle, E.3
  • 11
    • 0345800704 scopus 로고    scopus 로고
    • Ultrafast excited-state proton transfer of 2-(2′- hydroxyphenyl)benzothiazole: Theoretical analysis of the skeletal deformations and the active vibrational modes
    • R. de Vivie-Riedle V. De Waele L. Kurtz E. Riedle Ultrafast excited-state proton transfer of 2-(2′- hydroxyphenyl)benzothiazole: Theoretical analysis of the skeletal deformations and the active vibrational modes J. Phys. Chem. A 2003 107 10591 10599
    • (2003) J. Phys. Chem. A , vol.107 , pp. 10591-10599
    • De Vivie-Riedle, R.1    De Waele, V.2    Kurtz, L.3    Riedle, E.4
  • 12
    • 0000572986 scopus 로고
    • Laser-induced absorption and fluorescence studies of photochromic Schiff bases
    • K. Kownacki A. Mordzinski R. Wilbrandt A. Grabowska Laser-induced absorption and fluorescence studies of photochromic Schiff bases Chem. Phys. Lett. 1994 227 270 276
    • (1994) Chem. Phys. Lett. , vol.227 , pp. 270-276
    • Kownacki, K.1    Mordzinski, A.2    Wilbrandt, R.3    Grabowska, A.4
  • 13
    • 0002268483 scopus 로고
    • Photochromic anils. structure of photoisomers and thermal relaxation processes
    • T. Rosenfeld M. Ottolenghi A. Y. Meyer Photochromic Anils. Structure of Photoisomers and Thermal Relaxation Processes Mol. Photochem. 1973 5 39 60
    • (1973) Mol. Photochem. , vol.5 , pp. 39-60
    • Rosenfeld, T.1    Ottolenghi, M.2    Meyer, A.Y.3
  • 15
    • 33845282163 scopus 로고
    • A comprehensive investigation of the photophysics and photochemistry of salicylideneaniline and derivatives of phenylbenzothiazole including solvent effects
    • R. S. Becker C. Lenoble A. Zein A comprehensive investigation of the photophysics and photochemistry of salicylideneaniline and derivatives of phenylbenzothiazole including solvent effects J. Phys. Chem. 1987 91 3509 3517
    • (1987) J. Phys. Chem. , vol.91 , pp. 3509-3517
    • Becker, R.S.1    Lenoble, C.2    Zein, A.3
  • 16
    • 10844291888 scopus 로고    scopus 로고
    • Ultrafast excited-state dynamics in photochromic N-salicylideneaniline studied by femtosecond time-resolved REMPI spectroscopy
    • C. Okabe T. Nakabayashi Y. Inokuchi N. Nishi H. Sekiya Ultrafast excited-state dynamics in photochromic N-salicylideneaniline studied by femtosecond time-resolved REMPI spectroscopy J. Chem. Phys. 2004 121 9436 9442
    • (2004) J. Chem. Phys. , vol.121 , pp. 9436-9442
    • Okabe, C.1    Nakabayashi, T.2    Inokuchi, Y.3    Nishi, N.4    Sekiya, H.5
  • 17
    • 39749184620 scopus 로고    scopus 로고
    • Spectroscopic and photophysical studies of the hydroquinone family of photochromic Schiff bases analyzed over a 17-orders-of-magnitude time scale
    • M. Ziółek G. Burdziński K. Filipczak J. Karolczak A. Maciejewski Spectroscopic and photophysical studies of the hydroquinone family of photochromic Schiff bases analyzed over a 17-orders-of-magnitude time scale Phys. Chem. Chem. Phys. 2008 10 1304 1318
    • (2008) Phys. Chem. Chem. Phys. , vol.10 , pp. 1304-1318
    • Ziółek, M.1    Burdziński, G.2    Filipczak, K.3    Karolczak, J.4    MacIejewski, A.5
  • 18
    • 63849117885 scopus 로고    scopus 로고
    • Influence of intermolecular hydrogen bonding on the photochromic cycle of the aromatic schiff base n,n′-bis(salicylidene)-p-phenylenediamine in solution
    • M. Ziolek G. Burdzinski J. Karolczak Influence of Intermolecular Hydrogen Bonding on the Photochromic Cycle of the Aromatic Schiff Base N,N′-Bis(salicylidene)-p-phenylenediamine in Solution J. Phys. Chem. A 2009 113 2854 2864
    • (2009) J. Phys. Chem. A , vol.113 , pp. 2854-2864
    • Ziolek, M.1    Burdzinski, G.2    Karolczak, J.3
  • 19
    • 34547926019 scopus 로고    scopus 로고
    • Enol-keto tautomerism of aromatic photochromic Schiff base N,N′-bis(salicylidene)-p-phenylenediamine: Ground state equilibrium and excited state deactivation studied by solvatochromic measurements on ultrafast time scale
    • M. Ziółek J. Kubicki A. Maciejewski R. Naskrcki A. Grabowska Enol-keto tautomerism of aromatic photochromic Schiff base N,N′-bis(salicylidene)-p-phenylenediamine: Ground state equilibrium and excited state deactivation studied by solvatochromic measurements on ultrafast time scale J. Chem. Phys. 2006 124 124518
    • (2006) J. Chem. Phys. , vol.124 , pp. 124518
    • Ziółek, M.1    Kubicki, J.2    MacIejewski, A.3    Naskrcki, R.4    Grabowska, A.5
  • 20
    • 9744261730 scopus 로고    scopus 로고
    • Measurements of picosecond lifetimes by time correlated single photon counting method: The effect of the refraction index of the solvent on the instrument response function
    • T. Wróżowa B. Ciesielska D. Komar J. Karolczak A. Maciejewski J. Kubicki Measurements of picosecond lifetimes by time correlated single photon counting method: The effect of the refraction index of the solvent on the instrument response function Rev. Sci. Instrum. 2004 75 3107 3121
    • (2004) Rev. Sci. Instrum. , vol.75 , pp. 3107-3121
    • Wrózowa, T.1    Ciesielska, B.2    Komar, D.3    Karolczak, J.4    MacIejewski, A.5    Kubicki, J.6
  • 21
    • 71049194748 scopus 로고    scopus 로고
    • A. A. Granovsky, PC GAMESS/Firefly version 7.1.C, http://classic.chem. msu.su/gran/gamess/index.html, 2008
    • (2008) Gamess/firefly
    • Granovsky, P.C.1
  • 22
    • 33847797571 scopus 로고
    • The solvatochromic comparison method. 2. the alpha-scale of solvent hydrogen-bond donor (HBD) acidities
    • R. W. Taft M. J. Kamlet The solvatochromic comparison method. 2. The alpha-scale of solvent hydrogen-bond donor (HBD) acidities J. Am. Chem. Soc. 1976 98 2886 2894
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 2886-2894
    • Taft, R.W.1    Kamlet, M.J.2
  • 23
    • 0034743081 scopus 로고    scopus 로고
    • A study of the tautomers of N-salicylidene-p-X-aniline compounds in methanol
    • V. Vargas L. Amigo A study of the tautomers of N-salicylidene-p-X-aniline compounds in methanol J. Chem. Soc., Perkin Trans. 2 2001 1124 1129
    • (2001) J. Chem. Soc., Perkin Trans. 2 , pp. 1124-1129
    • Vargas, V.1    Amigo, L.2
  • 24
    • 84962419513 scopus 로고    scopus 로고
    • Tautomerism in hydroxynaphthaldehyde anils and azo analogues: A combined experimental and computational study
    • W. A. F. Fabian L. Antonov D. Nedeltcheva F. S. Kamounah P. J. Taylor Tautomerism in hydroxynaphthaldehyde anils and azo analogues: a combined experimental and computational study J. Phys. Chem. A 2004 108 7603 7612
    • (2004) J. Phys. Chem. A , vol.108 , pp. 7603-7612
    • Fabian, W.A.F.1    Antonov, L.2    Nedeltcheva, D.3    Kamounah, F.S.4    Taylor, P.J.5
  • 25
    • 0001518975 scopus 로고    scopus 로고
    • Solvent effect on intramolecular proton transfer equilibrium in some N-(R-salicylidene)-alkylamines
    • PII S002228600100638X
    • T. Dziembowska E. Jagodzinska Z. Rozwadowski M. Kotfica Solvent effect on intramolecular proton transfer equilibrium in some N-(R-salicylidene)- alkylamines J. Mol. Struct. 2001 598 229 234 (Pubitemid 33717233)
    • (2001) Journal of Molecular Structure , vol.598 , Issue.2-3 , pp. 229-234
    • Dziembowska, T.1    Jagodzinska, E.2    Rozwadowski, Z.3    Kotfica, M.4
  • 27
    • 63849130153 scopus 로고    scopus 로고
    • Hydrogen-Bonded Cyclic Dimer Formation in Temperature-Induced Reversal of Tautomerism of Salicylideneanilines
    • T. Fujiwara J. Harada K. Ogawa Hydrogen-Bonded Cyclic Dimer Formation in Temperature-Induced Reversal of Tautomerism of Salicylideneanilines J. Phys. Chem. A 2009 113 1822 1826
    • (2009) J. Phys. Chem. A , vol.113 , pp. 1822-1826
    • Fujiwara, T.1    Harada, J.2    Ogawa, K.3
  • 28
    • 41849091482 scopus 로고    scopus 로고
    • Temperature influence on the energy of nonspecific and specific interactions taking place between 4-aminophthalimide (4-AP) and homogeneous solvents
    • K. Dobek Temperature influence on the energy of nonspecific and specific interactions taking place between 4-aminophthalimide (4-AP) and homogeneous solvents Photochem. Photobiol. Sci. 2008 7 361 370
    • (2008) Photochem. Photobiol. Sci. , vol.7 , pp. 361-370
    • Dobek, K.1
  • 29
    • 0010779791 scopus 로고
    • Flash-photolysis of 2-(2′-hydroxyphenyl)-3-H-indole. Ground state keto-enol tautomerization by mutual hydrogen exchange and by proton catalysis
    • J. S. Stephan C. Ríos Rodríguez K. H. Grellmann K. A. Zachariasse Flash-photolysis of 2-(2′-hydroxyphenyl)-3-H-indole. Ground state keto-enol tautomerization by mutual hydrogen exchange and by proton catalysis Chem. Phys. 1994 186 435 446
    • (1994) Chem. Phys. , vol.186 , pp. 435-446
    • Stephan, J.S.1    Ríos Rodríguez, C.2    Grellmann, K.H.3    Zachariasse, K.A.4
  • 30
    • 35348981212 scopus 로고    scopus 로고
    • Ab Initio Investigation on the Second-Order Nonlinear Optical Responses in Keto-Enol Equilibria of Salicylideneanilines
    • M. Guillaume B. Champagne N. Markova V. Enchev F. Castet Ab Initio Investigation on the Second-Order Nonlinear Optical Responses in Keto-Enol Equilibria of Salicylideneanilines J. Phys. Chem. A 2007 111 9914 9923
    • (2007) J. Phys. Chem. A , vol.111 , pp. 9914-9923
    • Guillaume, M.1    Champagne, B.2    Markova, N.3    Enchev, V.4    Castet, F.5
  • 32
    • 33749124090 scopus 로고
    • Single versus double proton transfer in the photochromic Schiff bases. Electronic spectroscopy and synthesis of model compounds
    • K. Kownacki Ł. Kaczmarek A. Grabowska Single versus double proton transfer in the photochromic Schiff bases. Electronic spectroscopy and synthesis of model compounds Chem. Phys. Lett. 1993 210 373 379
    • (1993) Chem. Phys. Lett. , vol.210 , pp. 373-379
    • Kownacki, K.1    Kaczmarek, Ł.2    Grabowska, A.3


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