Origins of complex solvent effects on chemical reactivity and computational tools to investigate them: a review

Literature Information

Publication Date 2018-11-23
DOI 10.1039/C8RE00226F
Impact Factor 4.239
Authors

Jithin John Varghese, Samir H. Mushrif


View Original

Abstract

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

Experimental and theoretical study of the recombination reactions of FS(O2)O with FC(O)O and CO

M. E. Tucceri, M. P. Badenes, A. E. Croce, C. J. Cobos

2001-04-23 Paper

DOI: 10.1039/B100348H

Contents list

2021-08-10 Front/Back Matter

DOI: 10.1039/D1PY90107A

The effect of chiral end groups on the assembly of supramolecular polyurethanes

Daniel Hermida-Merino, Lewis R. Hart, Peter J. Harris, Andrew T. Slark, Ian W. Hamley, Wayne Hayes

2021-07-21 Paper

DOI: 10.1039/D1PY00714A

Highly 2,3-selective and fast living polymerization of alkyl-, alkoxy- and phenylallenes using nickel(ii) catalysts

Shu-Ming Kang, Xun-Hui Xu, Lei Xu, Li Zhou, Na Liu, Zong-Quan Wu

2021-07-27 Paper

DOI: 10.1039/D1PY00482D

Back cover

2021-08-17 Cover

DOI: 10.1039/D1PY90111G

Investigating the adsorption of anisotropic diblock copolymer worms onto planar silica and nanocellulose surfaces using a quartz crystal microbalance

Joakim Engström, Michael S. Reid, Emma E. Brotherton, Eva Malmström, Steven P. Armes, Fiona L. Hatton

2021-09-06 Paper

DOI: 10.1039/D1PY00644D

Inhibition of Jahn–Teller cooperative distortion in LiMn2O4 spinel by transition metal ion doping

Doretta Capsoni, Marcella Bini, Gaetano Chiodelli, Vincenzo Massarotti, Carlo B. Azzoni, Maria Cristina Mozzati, Alberto Comin

2001-05-10 Paper

DOI: 10.1039/B100080M

Highly stretchable, high efficiency room temperature self-healing polyurethane adhesive based on hydrogen bonds – applicable to solid rocket propellants

Tu Jing, Xu Heng, Xiang Guifeng, Chen Ling, Li Pingyun, Guo Xiaode

2021-07-12 Paper

DOI: 10.1039/D1PY00439E

Sequence-defined oligomer as a modular platform for selective sub-picomolar detection and removal of Hg2+

Anna Jose, Pandurangan Nanjan, Mintu Porel

2021-08-13 Paper

DOI: 10.1039/D1PY00642H

You might also like

Compound Q&A

What regulatory guidelines apply to 6-Bromo-2-methylimidazo[1,2-a]pyrimidine (CAS: 1111638-05-1)?

6-Bromo-2-methylimidazo[1,2-a]pyrimidine (CAS: 1111638-05-1) falls under various...

1111638-05-16-Bromo-2-methylimid...
Compound Q&A

Are there alternatives to 1-Pyrrolidineethanol, β-methyl-α-phenyl-, (αS,βR) (CAS: 123620-80-4) in synthesis?

While there are no direct alternatives, similar compounds like 1-Pyrrolidineetha...

123620-80-41-Pyrrolidineethanol...
Compound Q&A

Is 4-Methyl-2,6-bis(2-methyl-2-propanyl)phenyl methylcarbamate (CAS: 1918-11-2) safe?

4-Methyl-2,6-bis(2-methyl-2-propanyl)phenyl methylcarbamate (CAS: 1918-11-2) is ...

1918-11-24-Methyl-2,6-bis(2-m...
Compound Q&A

How should 2-(3-Bromo-4-fluorophenyl)-1,3-dioxolane (CAS: 77771-04-1) be stored?

2-(3-Bromo-4-fluorophenyl)-1,3-dioxolane (CAS: 77771-04-1) should be stored in a...

77771-04-12-(3-Bromo-4-fluorop...
Compound Q&A

What are the physical and chemical properties of 4,5,6,7-Tetrahydro-1H-indazole hydrochloride (CAS: 18161-11-0)?

4,5,6,7-Tetrahydro-1H-indazole hydrochloride is a white crystalline solid with a...

18161-11-04,5,6,7-Tetrahydro-1...
Compound Q&A

What is (2R)-1-Methoxy-3-phenyl-2-propanamine (CAS: 59919-07-2)?

(2R)-1-Methoxy-3-phenyl-2-propanamine is a chiral organic compound with the CAS ...

59919-07-2(2R)-1-Methoxy-3-phe...
Compound Q&A

What industries use Ethyl 1-(1-phenylethyl)-1H-imidazole-5-carboxylate (CAS: 56649-47-9)?

Ethyl 1-(1-phenylethyl)-1H-imidazole-5-carboxylate is used in various industries...

56649-47-9Ethyl 1-(1-phenyleth...
Compound Q&A

What regulatory guidelines apply to 4-[(1E,3S)-1-(4-Hydroxyphenyl)-1,4-pentadien-3-yl]phenol (CAS: 17676-24-3)?

4-[(1E,3S)-1-(4-Hydroxyphenyl)-1,4-pentadien-3-yl]phenol (CAS: 17676-24-3) falls...

17676-24-34-[(1E,3S)-1-(4-Hydr...
Compound Q&A

What industries use (S)-3-Amino-5-phenylpentanoic acid hydrochloride (CAS: 331846-97-0)?

(S)-3-Amino-5-phenylpentanoic acid hydrochloride is primarily used in the pharma...

331846-97-0(S)-3-Amino-5-phenyl...
Compound Q&A

How is 7-methoxy-1-benzothiophene-2-carboxylic acid (CAS: 88791-07-5) typically synthesized?

7-Methoxy-1-benzothiophene-2-carboxylic acid is typically synthesized by reactin...

88791-07-57-methoxy-1-benzothi...

Source Journal

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
Self-citation Rate: 8.8%
Articles per Year: 284

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.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.