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Journal of Physical Organic Chemistry is a peer-reviewed journal published by Wiley, covering Chemical Reaction Mechanisms, Photochemistry and Electron Transfer Studies, Free Radicals and Antioxidants.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Journal of Physical Organic Chemistry 12 (3): 45–58.
Formats any DOI in Journal of Physical Organic Chemistry style. No sign-up. |
| Publishes research in | Chemical Reaction Mechanisms Photochemistry and Electron Transfer Studies Free Radicals and Antioxidants Advanced Chemical Physics Studies Organic Chemistry Cycloaddition Reactions |
| ISSN | 0894-3230 |
| Citation impact (2-yr) | 1.16 |
| h-index | 87 |
| i10-index | 2,092 |
| Total citations | 71,689 |
| Article processing charge | $3,660 |
| Top institutions publishing here | Centre National de la Recherche Scientifique |
| Journal website | onlinelibrary.wiley.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Abstract Ionic liquids are a fascinating class of novel solvents, which are attracting attention as possible ‘green’ alternative to volatile molecular organic solvents to be applied in catalytic and organic reactions and electrochemical and separation processes. Over 200 room temperature ionic liquids are known but for most of them physico‐chemical data are incomplete or lacking.…
The polarity of ambient-temperature ionic liquids based on the 1-alkyl-3-methylimidazolium cation was probed using the solvatochromic dye Nile Red. The polarity of these liquids was shown to be comparable to that of the lower alcohols. The effects on polarity with changing anion and 1-alkyl group are reported. Copyright © 2000 John Wiley & Sons, Ltd.
Molecular mutagens and carcinogens are structures which carry chemical and electronic properties that disturb and interact with the genomic machinery. Principally, a rule of thumb for carcinogens is that carcinogens are expected to introduce covalent irreversible bonding to one or several types of DNA bases, causing errors in the reading frame for the polymerases. 8‐methoxy‐6‐nitrophenanthro[3,4‐d][1,3]dioxole‐5‐carboxylic…
Abstract Different methods of estimating H‐bond strength are presented. The studies are based on the results of MP2/6–311++G** calculations and the binding energies are corrected for the basis set superposition error (BSSE). The wavefunctions were further applied to localize bond critical points and ring critical points. The characteristics based on the Bader theory are also…
Abstract This paper reports the application of the recently proposed formalism known as generalized population analysis (GPA) as a new means for the quantitative characterization of the aromaticity of various benzenoid rings in polycyclic aromatic hydrocarbons (PAHs). The quantity which we propose as a new measure of aromaticity is the so‐called six‐center bond index. The…
