This review provides an overview of the chemistry, structure and potential applications of 1- (acyl/aroyl)-3-(mono-substituted) and 1-(acyl/aroyl)-3,3-(di-substituted) thioureas, with general formula R1C(O)N(1)HC(S)N(3)R2R3. In recent years, the title compounds have found extensive applications as ligands in coordination chemistry. The effect that nitrogen substituents exert on the intra- and intermolecular hydrogen-bonding interactions is discussed, including their role…
Journal of Sulfur Chemistry Template
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About the Journal of Sulfur Chemistry format
Journal of Sulfur Chemistry is a peer-reviewed journal published by Taylor & Francis, covering Sulfur-Based Synthesis Techniques, Synthesis and biological activity, Chemical Synthesis and Reactions.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Numbered (Vancouver/NLM) Numbered — [1], [2] in the text 1. Smith A, Jones B, Lee C. A representative article title. Journal of Sulfur Chemistry. 2023;12(3):45–58.
Formats any DOI in Journal of Sulfur Chemistry style. No sign-up. |
| Publishes research in | Sulfur-Based Synthesis Techniques Synthesis and biological activity Chemical Synthesis and Reactions Synthesis of heterocyclic compounds Multicomponent Synthesis of Heterocycles |
| ISSN | 1741-5993 |
| Citation impact (2-yr) | 1.86 |
| h-index | 40 |
| i10-index | 441 |
| Total citations | 13,812 |
| Top institutions publishing here | Payame Noor University |
| Journal website | www.tandfonline.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Journal of Sulfur Chemistry per year
Citation impact of Journal of Sulfur Chemistry by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Journal of Sulfur Chemistry
The disproportionation of inorganic sulfur intermediates at moderate temperatures (0-80 °C) is a microbiologically catalyzed chemolithotrophic process in which compounds like elemental sulfur, thiosulfate, and sulfite serve as both electron donor and acceptor, and generate hydrogen sulfide and sulfate. Thus the overall process is comparable to the fermentation of organic compounds such as glucose and…
Thioesters are important class of organosulfur compounds that play a fundamental role in the construction of pharmaceutical, biological, industrial and natural products. In this respect, thioesters synthesis is one of the most important tasks in organosulfur chemistry. The esterification of thiols is the best and most common strategy for the synthesis of thioesters. During the…
We studied the adsorption of SOx (x = 2,3) molecules on the surface of pristine graphene (PG) and N-doped graphene (NDG) by density functional theory (DFT) calculations at the B3LYP/6-31G(d) level. We used Mulliken and NBO charge analysis to calculate the net charge transfer of adsorbed SOx on pristine and defected graphene systems. Our calculations…
The class of heterocyclic compounds known as thiazole is found in many natural and synthetic products with a wide range of pharmacological activities, such as antiviral, anticancer, antibacterial, antifungal, anticonvulsant, antiparkinsonian and anti-inflammatory activities that can be well illustrated by the large number of drugs in the market containing this function group. Due to its…