Karel G Von Eschwege

Dr. Karel G Von Eschwege

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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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6 June 2011 in Journal of Physical Organic Chemistry
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Journal Article
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AKAnnemarie Kuhn
Annemarie Kuhn
KEKarel G Von Eschwege
Karel G Von Eschwege
JCJeanet Conradie
Jeanet Conradie

3 April 2023 in ACS Omega
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Journal Article
Open access
NANigussie Alebachew
Nigussie Alebachew
HMH C Ananda Murthy
H C Ananda Murthy
BGBedasa Abdisa Gonfa
Bedasa Abdisa Gonfa
KEKarel G Von Eschwege
Karel G Von Eschwege
ELErnst HG Langner
Ernst HG Langner
TDTaye B. Demissie
Taye B. Demissie

21 November 2011 in The Journal of Physical Chemistry A
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Journal Article
Closed access
KEKarel G Von Eschwege
Karel G Von Eschwege
JCJeanet Conradie
Jeanet Conradie
AKAnnemarie Kuhn
Annemarie Kuhn

1 October 2016 in Electrochimica Acta
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Journal Article
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HFHendrik Ferreira
Hendrik Ferreira
KEKarel G Von Eschwege
Karel G Von Eschwege
JCJeanet Conradie
Jeanet Conradie

7 September 2020 in Electroanalysis
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Journal Article
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DWDeidré van der Westhuizen
Deidré van der Westhuizen
JCJeanet Conradie
Jeanet Conradie
KEKarel G Von Eschwege
Karel G Von Eschwege

21 November 2017 in The Journal of Physical Chemistry A
Verified
Journal Article
Open access
LNLumanyano L. A. Ntoi
Lumanyano L. A. Ntoi
BBBlenerhassitt E. Buitendach
Blenerhassitt E. Buitendach
KEKarel G Von Eschwege
Karel G Von Eschwege
Variations in the electromagnetic wavelengths of absorption and reflection of molecules do not only make life colorful but also are often of central importance in solar energy conversion and optoelectronic information processing and transfer. Dithizone and its derivatives and complexes are, to our knowledge, probably the most “colorful” compound, being responsive to no less than seven different external stimuli that effect color change. Apart from a more detailed discussion of the cyclic voltammetry and observed electrochromism in the SCH3-substituted free ligand and mercury complex, concentratochromism, solvatochromism, halochromism, thermochromism, and chronochromism in the ligand, and photochromism in the carboxy-functionalized phenylmercury(II) complex are also presented here. Color changes are either associated with proton transfer or loss, or isomerization.