Jose Maria Alvarez Pez

Dr. Jose Maria Alvarez Pez

Extraordinary Collaborator of the Physical Chemistry Department, University of Granada, 18071 Granada, Spain

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 August 2011 in Chemistry – A European Journal
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Journal Article
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NBNoël Boens
Noël Boens
WQWenwu Qin
Wenwu Qin
MBMukulesh Baruah
Mukulesh Baruah
Wim Michel De BorggraeveWim Michel De Borggraeve
Wim Michel De Borggraeve
Aleksander FilarowskiAleksander Filarowski
Aleksander Filarowski
Jose Maria Alvarez PezJose Maria Alvarez Pez
Jose Maria Alvarez Pez

3 January 2006 in Chromatographia
Verified
Journal Article
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RBR. Bermejo
R. Bermejo
MFM. A. Felipe
M. A. Felipe
ETE. M. Talavera
E. M. Talavera
Jose Maria Alvarez PezJose Maria Alvarez Pez
Jose Maria Alvarez Pez

25 June 2013 in The Journal of Physical Chemistry B
Verified
Journal Article
Closed access
JPJosé Manuel Paredes
José Manuel Paredes
María Dolores Girón GonzálezMaría Dolores Girón González
María Dolores Girón González
Maria J. Ruedas-RamaMaria J. Ruedas-Rama
Maria J. Ruedas-Rama
Angel OrteAngel Orte
Angel Orte
LGLuis Crovetto González
Luis Crovetto González
Jose Maria Alvarez PezJose Maria Alvarez Pez
Jose Maria Alvarez Pez

6 October 2011 in Langmuir
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Journal Article
Closed access
Angel OrteAngel Orte
Angel Orte
Maria J. Ruedas-RamaMaria J. Ruedas-Rama
Maria J. Ruedas-Rama
JPJosé Manuel Paredes
José Manuel Paredes
LGLuis Crovetto González
Luis Crovetto González
Jose Maria Alvarez PezJose Maria Alvarez Pez
Jose Maria Alvarez Pez

23 April 2009 in Physical Chemistry Chemical Physics
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Journal Article
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JPJosé Manuel Paredes
José Manuel Paredes
LGLuis Crovetto González
Luis Crovetto González
RTRamon Rios Torres
Ramon Rios Torres
Angel OrteAngel Orte
Angel Orte
Jose Maria Alvarez PezJose Maria Alvarez Pez
Jose Maria Alvarez Pez
ETEva M. Talavera
Eva M. Talavera
The photophysical behaviour of the new fluorescein derivative 9-[1-(2-methyl-4-methoxyphenyl)]-6-hydroxy-3H-xanthen-3-one has been explored by using absorption, and steady-state, time-resolved and single-molecule fluorescence measurements. The apparent ground-state acidity constant of the dye determined by both the absorbance and steady-state fluorescence is almost independent of the added buffer and salt concentrations. The excited-state proton exchange reaction around the physiological pH becomes reversible upon addition of phosphate buffer, inducing a pH-dependent change of the steady-state fluorescence and decay times. Fluorescence decay traces, collected as a function of total buffer concentration and pH, were analyzed by global compartmental analysis (GCA) to elucidate the values of the excited-state rate constants. The features of this system make the fluorescence decays monoexponential at pH values and phosphate buffer concentrations higher than 6.10 and 0.2 M respectively, with the possibility of tuning the fluorescence lifetime value by changing pH or buffer concentrations. The tuned lifetimes obtained by means of phosphate concentration at constant pH have also been recovered at the single-molecule level.

8 December 2009 in The Journal of Physical Chemistry B
Verified
Journal Article
Closed access
Maria J. Ruedas-RamaMaria J. Ruedas-Rama
Maria J. Ruedas-Rama
Angel OrteAngel Orte
Angel Orte
LGLuis Crovetto González
Luis Crovetto González
ETEva M. Talavera
Eva M. Talavera
Jose Maria Alvarez PezJose Maria Alvarez Pez
Jose Maria Alvarez Pez