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Volumn 16, Issue 29, 2010, Pages 8822-8831

2-Hydroxyazobenzenes to tailor pH Pulses and oscillations with light

Author keywords

Acidity; Azo compounds; Isomerization; Photochromism; Protonation

Indexed keywords

AZO COMPOUND; AZO COMPOUNDS; CROSS SECTION; H NMR SPECTROSCOPY; MONOCHROMATIC LIGHT; PH DROP; PH OSCILLATIONS; PHENOL GROUPS; PROTON CONCENTRATIONS; SINGLE WAVELENGTH; STEADY-STATE FLUORESCENCE; THERMAL BACK-ISOMERIZATION; TIME-SCALES;

EID: 77955126007     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201000541     Document Type: Article
Times cited : (49)

References (66)
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    • 3 when R becomes more and more electron withdrawing. However the slope value that is larger than 1 suggests that the position subjected to the R influence is close to the substituted phenyl, ring
    • 3 when R becomes more and more electron withdrawing. However the slope value that is larger than 1 suggests that the position subjected to the R influence is close to the substituted phenyl, ring.
  • 48
    • 0003399306 scopus 로고
    • Eds.: H. Dürr, H. Bouas-Laurent, Elsevier, Amsterdam
    • H. Rau, Photochromism: Molecules and Systems (Eds.: H. Dürr, H. Bouas-Laurent), Elsevier, Amsterdam, 1990.
    • (1990) Photochromism: Molecules and Systems
    • Rau, H.1
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  • 54
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    • T→C (347)
    • T→C (347).
  • 66
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    • Gnu Scientific Library, http://www.gnu.org/software/gsl/.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.