Origins of complex solvent effects on chemical reactivity and computational tools to investigate them: a review
Literature Information
Jithin John Varghese, Samir H. Mushrif
Solvents are crucial components in specialty chemical and pharmaceutical industries and in electrochemical and photoelectrochemical processes, and are increasingly being used in catalytic reactions. Solvents significantly influence the kinetics and thermodynamics of reactions and can alter product selectivity markedly. While such solvent effects are observed routinely, identification of the root causes of such effects is less frequent. Solvents can influence reaction rates, conversion and product selectivity by 1) directly participating in the reaction steps and opening alternate reaction pathways, 2) competing with the reactant for interaction with the catalysts, 3) changing the relative stabilization of the reactant, the transition state (TS) and/or the product, 4) altering intra-pore diffusion characteristics in porous catalysts, 5) exhibiting entropic confinement effects altering free energy barriers of reactions, 6) changing the solubility of different components in the reaction mixture, and 7) inhibiting undesired reactions. Their indirect influences may be due to 1) changes brought on to active sites on catalysts and 2) altered structure/stability of catalysts. This article discusses these fundamental reasons behind observed solvent effects with suitable examples. Advances in computational chemistry have led to the development of multiple tools and techniques, considering solvents either as implicit or as explicit molecules, providing molecular insights into complex solvent effects in catalysis. This article provides an overview of some of these methods with suitable examples to demonstrate their application and potential. This mapping of the solvent effects and their origins is believed to aid in the rational selection of solvents for catalytic reactions. The description of the computational tools, their application and their potential is likely to encourage widespread use of these techniques to investigate solvent effects.
Related Literature
Bisucaberin biosynthesis: an adenylating domain of the BibC multi-enzyme catalyzes cyclodimerization of N-hydroxy-N-succinylcadaverine
DOI: 10.1039/B813029A
Self-assembly of amphiphilic poly(phenylene ethynylene)s in water–potassium dodecanoate–decanol lyotropic liquid crystals
Jean Bouffard, Timothy M. Swager
DOI: 10.1039/B814598A
Quantifying the fraction of glycine and alanine in β-sheet and helical conformations in spider dragline silk using solid-state NMR
Gregory P. Holland, Janelle E. Jenkins, Melinda S. Creager, Randolph V. Lewis, Jeffery L. Yarger
DOI: 10.1039/B812928B
Novel highly active FSM-16 supported molybdenum catalyst for hydrotreatment
Shelu Garg, Thallada Bhaskar, Kapil Soni, Gnanamani Muthu Kumaran, Akinori Muto, Yusaku Sakata, Gudimella Murali Dhar
DOI: 10.1039/B809808E
Amino-sugar modular ligands—useful cores for the formation of asymmetric copper 1,4-addition catalysts
Antonella De Roma, Francesco Ruffo, Simon Woodward
DOI: 10.1039/B813137F
Templating effect of silk fibers in the oriented deposition of aragonite
Cheng Cheng, Yuhong Yang, Xin Chen, Zhengzhong Shao
DOI: 10.1039/B810337B
Facile synthesis of aminophenylboronic acid-functionalized magnetic nanoparticles for selective separation of glycopeptides and glycoproteins
Wei Zhou, Ning Yao, Guoping Yao, Chunhui Deng, Xiangmin Zhang, Pengyuan Yang
DOI: 10.1039/B808800D
A genetic selection system for evolving enantioselectivity of enzymes
Manfred T. Reetz, Horst Höbenreich, Pankaj Soni, Layla Fernández
DOI: 10.1039/B814538E
An unexpected ruthenium complex and its unique behavior as catalyst in dynamic kinetic resolution of secondary alcohols‡
Qihui Chen, Chengye Yuan
DOI: 10.1039/B811627J
Click chemistry assembly of G-quadruplex ligands incorporating a diarylurea scaffold and triazole linkers
William C. Drewe, Stephen Neidle
DOI: 10.1039/B814576H
You might also like
What are the main uses of 1H-Indazole-6-carbonitrile (CAS: 141290-59-7)?
1H-Indazole-6-carbonitrile finds applications in pharmaceuticals, where it serve...
How should waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) be handled?
Waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) should be collecte...
What industries use Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide (CAS: 68291-98-5)?
Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide is primarily used in pharmac...
Are there alternatives to Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxylate (CAS: 741709-66-0) in synthesis?
Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxyla...
How should waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) be handled?
Waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) should be manage...
What is 6-Formyl-2-pyridinecarboxylic acid (CAS: 499214-11-8)?
6-Formyl-2-pyridinecarboxylic acid is an organic compound with the molecular for...
What is the market or research trend for 3-(3,4-dimethoxyphenyl)-2,5-dimethyl-N-(2-morpholin-4-ylethyl)pyrazolo[1,5-a]pyrimidin-7-amine (CAS: 900874-91-1)?
Research trends for this compound indicate a focus on its potential applications...
How is 9H-Tribenzo[b,d,f]azepine (CAS: 29875-73-8) typically synthesized?
9H-Tribenzo[b,d,f]azepine is typically synthesized via a multi-step process invo...
How is 1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid (CAS: 1797982-51-4) typically synthesized?
1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxyli...
How should waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: 671820-52-3) be handled?
Waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: ...
Source Journal
Reaction Chemistry & Engineering

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.














