Cage effect in supercritical fluids and compressed gases in the photolysis of an asymmetrically substituted diazene

We studied the photolysis of (1-biphenyl-4-yl-1-methyl-ethyl)-tert-butyl diazene in supercritical CO2 and Xe, as well as in compressed Kr. The compound has good solubility in the mentioned fluids, allowing the photolysis measurements to be performed in CO2 at 1.4 K above Tc and at pressures as low a...

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Autor principal: Hoijemberg, P.A
Otros Autores: Zerbs, J., Japas, M.L, Chesta, C.A, Schroeder, J., Aramendia, P.F
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2009
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024 7 |2 cas  |a imide, 32323-01-6; (1-biphenyl-4-yl-1-methylethyl)-tert-butyl diazene; Biphenyl Compounds; Gases; Imides 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JPCAF 
100 1 |a Hoijemberg, P.A. 
245 1 0 |a Cage effect in supercritical fluids and compressed gases in the photolysis of an asymmetrically substituted diazene 
260 |c 2009 
270 1 0 |m Aramendia, P. F.; INQUIMAE, Departamento de Quimica Inorganica, Analitica y Quimica Fisica, Universidad de Buenos Aires, Pabellon 2, Ciudad Universitaria, 1428 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
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504 |a Hoijemberg, P.A., Zerbs, J., Reichardt, C., Schwarzer, D., Chesta, C.A., Schroeder, J., Aramendia, P.F., Photophysics and photochemistry of an asymmetrically substituted diazene: An adequate cage effect probe. J. Phys. Chem. A, , accepted for publication 
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520 3 |a We studied the photolysis of (1-biphenyl-4-yl-1-methyl-ethyl)-tert-butyl diazene in supercritical CO2 and Xe, as well as in compressed Kr. The compound has good solubility in the mentioned fluids, allowing the photolysis measurements to be performed in CO2 at 1.4 K above Tc and at pressures as low as 70 bar. We monitored relative cage effect after nanosecond laser pulses by measuring the absorbance at 320 nm (AAtf 0) corresponding to the total amount of out-of-cage 1-biphenyl-4-yl-1-methyl-ethyl radical (BME ·) produced after nitrogen loss of the diazene. In supercritical CO2 and Xe, isothermal values of AAtf 0 showed an increase-decrease behavior with increasing pressure at constant temperature, a typical feature of the transition from the solvent energy transfer to the friction controlled regimes. The comparison of the behavior of AAtf 0 in CO2 at reduced temperatures between 1.004 and 1.027, in Xe, and in Kr points to an absence of enhanced cage effect near the critical point. Compatibility with spectroscopic data is analyzed. © 2009 American Chemical Society.  |l eng 
593 |a INQUIMAE, Departamento de Quimica Inorganica, Analitica y Quimica Fisica, Universidad de Buenos Aires, Pabellon 2, Ciudad Universitaria, 1428 Buenos Aires, Argentina 
593 |a Institut für Physikalische Chemie, Georg-August Universität, Gottingen, Germany 
593 |a UAQ, CNEA, UNSAM, Argentina 
593 |a Departamento de Quimica Facultad de Ciencias Exactas, Fisicoquimicas y Naturales, Universidad Nacional de Rio Cuarto, 5800-Rio Cuarto, Argentina 
593 |a Institut für Verbrennungstechnik, Deutsche Gesellschaft Für Luft- and Raumfahrt, Stuttgart, Germany 
690 1 0 |a ABSORBANCE 
690 1 0 |a CAGE EFFECT 
690 1 0 |a COMPRESSED GAS 
690 1 0 |a CONSTANT TEMPERATURE 
690 1 0 |a CRITICAL POINTS 
690 1 0 |a DIAZENE 
690 1 0 |a ETHYL RADICALS 
690 1 0 |a NANOSECOND LASER PULSE 
690 1 0 |a NITROGEN LOSS 
690 1 0 |a SPECTROSCOPIC DATA 
690 1 0 |a SUPERCRITICAL CO2 
690 1 0 |a EFFLUENT TREATMENT 
690 1 0 |a ENERGY TRANSFER 
690 1 0 |a EQUATIONS OF STATE 
690 1 0 |a KRYPTON 
690 1 0 |a ORGANIC POLYMERS 
690 1 0 |a PULSED LASER APPLICATIONS 
690 1 0 |a SUPERCRITICAL FLUIDS 
690 1 0 |a TECHNETIUM 
690 1 0 |a PHOTOLYSIS 
690 1 0 |a (1 BIPHENYL 4 YL 1 METHYLETHYL) TERT BUTYL DIAZENE 
690 1 0 |a (1-BIPHENYL-4-YL-1-METHYLETHYL)-TERT-BUTYL DIAZENE 
690 1 0 |a BIPHENYL DERIVATIVE 
690 1 0 |a IMIDE 
690 1 0 |a ABSORPTION 
690 1 0 |a ARTICLE 
690 1 0 |a CHEMISTRY 
690 1 0 |a GAS 
690 1 0 |a PHOTOLYSIS 
690 1 0 |a SOLUBILITY 
690 1 0 |a ABSORPTION 
690 1 0 |a BIPHENYL COMPOUNDS 
690 1 0 |a IMIDES 
690 1 0 |a PHOTOLYSIS 
690 1 0 |a SOLUBILITY 
650 1 7 |2 spines  |a XENON 
650 1 7 |2 spines  |a GASES 
700 1 |a Zerbs, J. 
700 1 |a Japas, M.L. 
700 1 |a Chesta, C.A. 
700 1 |a Schroeder, J. 
700 1 |a Aramendia, P.F. 
773 0 |d 2009  |g v. 113  |h pp. 5289-5295  |k n. 18  |p J Phys Chem A  |x 10895639  |t Journal of Physical Chemistry A 
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856 4 0 |u https://doi.org/10.1021/jp811390m  |y DOI 
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