Hem Joshi

Dr. Hem Joshi

Institute for Plasma Research
orcid

Research Focus & Metrics

Academic Career Length

39Years (1988-Present)

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

Representative Publications

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9 March 2021 in Molecules
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Journal Article
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HJHem Joshi
Hem Joshi
Liudmil AntonovLiudmil Antonov
Liudmil Antonov
In this short review, we attempt to unfold various aspects of excited-state intramolecular proton transfer (ESIPT) from the studies that are available up to date. Since Weller’s discovery of ESIPT in salicylic acid (SA) and its derivative methyl salicylate (MS), numerous studies have emerged on the topic and it has become an attractive field of research because of its manifold applications. Here, we discuss some critical aspects of ESIPT and tautomerization from the mechanistic viewpoint. We address excitation wavelength dependence, anti-Kasha ESIPT, fast and slow ESIPT, reversibility and irreversibility of ESIPT, hydrogen bonding and geometrical factors, excited-state double proton transfer (ESDPT), concerted and stepwise ESDPT.

1 September 2002 in Journal of Photochemistry and Photobiology A: Chemistry
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Journal Article
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HJHem Joshi
Hem Joshi
FKFadhil S. Kamounah
Fadhil S. Kamounah
CGCees Gooijer
Cees Gooijer
GZGert van der Zwan
Gert van der Zwan
Liudmil AntonovLiudmil Antonov
Liudmil Antonov

1 July 1994 in Chemical Physics
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Journal Article
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DPD.D. Pant
D.D. Pant
HJHem Joshi
Hem Joshi
PBP.B. Bisht
P.B. Bisht
HTH.B. Tripathi
H.B. Tripathi

5 November 2001 in Journal of the Chemical Society, Perkin Transactions 2
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Journal Article
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HJHem Joshi
Hem Joshi
FKFadhil S. Kamounah
Fadhil S. Kamounah
GZGert van der Zwan
Gert van der Zwan
CGCees Gooijer
Cees Gooijer
Liudmil AntonovLiudmil Antonov
Liudmil Antonov
The spectral properties of several aromatic azo dyes of fundamental importance (4-phenylazo-1-naphthol, 1-phenylazo-2-naphthol and 2-phenylazo-1-naphthol) and Schiff bases (N-(2-hydroxy-1-naphthylmethylidene)aniline and N-(1-hydroxy-2-naphthylmethylidene)aniline) are investigated at temperatures down to 100 K. The observed spectral changes are interpreted in terms of the existing tautomeric equilibrium and hydrogen-bonding (H-bonding) with the solvent. In non-polar solvents the decrease in temperature leads, in all compounds except 4-phenylazo-1-naphthol, to a full transformation of the enol tautomeric form (A) to the quinone form (H). The temperature dependence of the equilibrium A ⇌ H exhibits a shift around 240 K. In ethanol, due to intermolecular H-bonding, in the case of the azo dyes full transformation was not observed, while the behavior of the Schiff bases is the same as in non-polar solvents. The thermodynamic parameters of the equilibrium A ⇌ H were estimated in both non-polar solvent and ethanol for all investigated compounds.

1 February 2001 in Journal of Photochemistry and Photobiology A: Chemistry
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HMHirdyesh Mishra
Hirdyesh Mishra
HJHem Joshi
Hem Joshi
HTHira Ballabh Tripathi
Hira Ballabh Tripathi
SMShruti Maheshwary
Shruti Maheshwary
NSNarayanasami Sathyamurthy
Narayanasami Sathyamurthy
JCJayaraman Chandrasekhar
Jayaraman Chandrasekhar

23 March 2023 in Applied Spectroscopy Reviews
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Journal Article
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JTJinto Thomas
Jinto Thomas
HJHem Joshi
Hem Joshi
In this review, we attempt to provide a brief account of laser-induced breakdown spectroscopy (LIBS) methodology and technological developments. We also summarize various methods adopted for exploiting LIBS. Besides, a brief overview of combination of LIBS in conjunction with other methods is also given.