Imperial College London

Professor Tom Welton

Faculty of Natural SciencesDepartment of Chemistry

Professor of Sustainable Chemistry
 
 
 
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Contact

 

+44 (0)20 7594 5763t.welton Website

 
 
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Location

 

601AMolecular Sciences Research HubWhite City Campus

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Summary

 

Publications

Publication Type
Year
to

255 results found

Skarmoutsos I, Dellis D, Matthews RP, Welton T, Hunt PAet al., 2012, Hydrogen Bonding in 1-Butyl- and 1-Ethyl-3-methylimidazolium Chloride Ionic Liquids, The Journal of Physical Chemistry B, Vol: 116, Pages: 4921-4933-4921-4933

Journal article

Niedermeyer H, Hallett JP, Villar-Garcia IJ, Hunt PA, Welton Tet al., 2012, Mixtures of ionic liquids, CHEMICAL SOCIETY REVIEWS, Vol: 41, Pages: 7780-7802, ISSN: 0306-0012

Journal article

Ab Rani MA, Brandt A, Crowhurst L, Dolan A, Hassan NH, Hallett JP, Hunt PA, Lui M, Niedermeyer H, Perez-Arlandis JM, Schrems M, To TQ, Welton T, Wilding Ret al., 2011, Erratum: Understanding the polarity of ionic liquids (Physical Chemistry Chemical Physics (2011) DOI: 10.1039/c1cp21262a), Physical Chemistry Chemical Physics, Vol: 13, ISSN: 1463-9076

Journal article

Hallett JP, Welton T, 2011, Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2, CHEMICAL REVIEWS, Vol: 111, Pages: 3508-3576, ISSN: 0009-2665

Journal article

Schrems Michael, Brandt Agnieszka, Welton Tom, Liebner Falk, Rosenau Thomas, Potthast Antjeet al., 2011, Ionic liquids as media for biomass processing: opportunities and restrictions

Conference paper

Ab Rani MA, Brant A, Crowhurst L, Dolan A, Lui M, Hassan NH, Hallett JP, Hunt PA, Niedermeyer H, Perez-Arlandis JM, Schrems M, Welton T, Wilding Ret al., 2011, Understanding the polarity of ionic liquids, Phys. Chem. Chem. Phys., Vol: 13, Pages: 16831-16840-16831-16840

The polarities of a wide range of ionic liquids have been determined using the Kamlet-Taft empirical polarity scales [small alpha], [small beta] and [small pi]*, with the dye set Reichardt’s Dye, N,N-diethyl-4-nitroaniline and 4-nitroaniline. These have been compared to measurements of these parameters with different dye sets and to different polarity scales. The results emphasise the importance of recognising the role that the nature of the solute plays in determining these scales. It is particularly noted that polarity scales based upon charged solutes can give very different values for the polarity of ionic liquids compared to those based upon neutral probes. Finally, the effects of commonplace impurities in ionic liquids are reported.

Journal article

Brandt A, Ray MJ, To TQ, Leak DJ, Murphy RJ, Welton Tet al., 2011, Ionic liquid pretreatment of lignocellulosic biomass with ionic liquid-water mixtures, Green Chem., Vol: 13, Pages: 2489-2499-2489-2499

Ground lignocellulosic biomass (Miscanthus giganteus, pine (Pinus sylvestris) and willow (Salix viminalis)) was pretreated with ionic liquid-water mixtures of 1-butyl-3-methylimidazolium methyl sulfate and 1-butyl-3-methylimidazolium hydrogen sulfate. A solid fraction enriched in cellulose was recovered, which was subjected to enzymatic hydrolysis. Up to 90% of the glucose and 25% of the hemicellulose contained in the original biomass were released by the combined ionic liquid pretreatment and the enzymatic hydrolysis. After the pretreatment, the ionic liquid liquor contained the majority of the lignin and the hemicellulose. The lignin portion was partially precipitated from the liquor upon dilution with water. The amount of hemicellulose monomers in the ionic liquid liquor and their conversion into furfurals was also examined. The performance of ionic liquid-water mixtures containing 1,3-dialkylimidazolium ionic liquids with acetate, methanesulfonate, trifluoromethanesulfonate and chloride anions was investigated. The applicability of the ionic liquid 1-butylimidazolium hydrogensulfate for lignocellulose pretreatment was also examined. It was found that ionic liquid liquors containing methyl sulfate, hydrogen sulfate and methanesulfonate anions were most effective in terms of lignin/cellulose fractionation and enhancement of cellulose digestibility.

Journal article

Ab Rani MA, Brandt A, Crowhurst L, Dolan A, Hassan NH, Hallett JP, Hunt PA, Lui M, Niedermeyer H, Perez-Arlandis JM, Schrems M, To TQ, Welton T, Wilding Ret al., 2011, Understanding the polarity of ionic liquids (vol 13, pg 16831, 2011), PHYSICAL CHEMISTRY CHEMICAL PHYSICS, Vol: 13, Pages: 21653-21653, ISSN: 1463-9076

Journal article

Perkin S, Crowhurst L, Niedermeyer H, Welton T, Smith AM, Gosvami NNet al., 2011, Self-assembly in the electrical double layer of ionic liquids, CHEMICAL COMMUNICATIONS, Vol: 47, Pages: 6572-6574, ISSN: 1359-7345

Journal article

Welton T, 2011, Ionic liquids in <i>Green Chemistry</i>, GREEN CHEMISTRY, Vol: 13, Pages: 225-225, ISSN: 1463-9262

Journal article

Lui MY, Crowhurst L, Hallett JP, Hunt PA, Niedermeyer H, Welton Tet al., 2011, Salts dissolved in salts: ionic liquid mixtures, Chem. Sci., Vol: 2, Pages: 1491-1496-1491-1496

Journal article

Reichardt C, Welton T, 2010, Solvents and Solvent Effects in Organic Chemistry, Publisher: Wiley-VCH, ISBN: 9783527324736

Book

Reichardt C, Welton T, 2010, Solvents and Solvent Effects in Organic Chemistry: Fourth Edition, ISBN: 9783527324736

Now in its 4th edition, this book remains the ultimate reference for all questions regarding solvents and solvent effects in organic chemistry. Retaining its proven concept, there is no other book which covers the subject in so much depth, the handbook is completely updated and contains 15% more content, including new chapters on "Solvents and Green chemistry", "Classification of Solvents by their Environmental Impact", and "Ionic Liquids". An essential part of every organic chemist's library. © 2011 Wiley-VCH Verlag GmbH & Co. KGaA.

Book

Hunt P, Niedermeyer H, Welton T, 2010, What happens when you functionalise an ionic liquid with a "silicone" side chain?, ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, Vol: 239, ISSN: 0065-7727

Journal article

Brandt A, Hallett JP, Leak DJ, Murphy RJ, Welton Tet al., 2010, The effect of the ionic liquid anion in the pretreatment of pine wood chips, Green Chem., Vol: 12, Pages: 672-679-672-679

The effect of the anion of ionic liquids on air-dried pine (Pinus radiata) has been investigated. All ionic liquids used in this study contained the 1-butyl-3-methylimidazolium cation; the anions were trifluoromethanesulfonate, methylsulfate, dimethylphosphate, dicyanamide, chloride and acetate. Using a protocol for assessing the ability to swell small wood blocks (10 [times] 10 [times] 5 mm), it was shown that the anion has a profound impact on the ability to promote both swelling and dissolution of biomass. Time course studies showed that viscosity, temperature and water content were also important parameters influencing the swelling process. We used Kamlet-Taft parameters to quantify the solvent polarity of the ionic liquids and found that the anion basicity described by the parameter [small beta] correlated with the ability to expand and dissolve pine lignocellulose. It is shown that 1-butyl-3-methylimidazolium dicyanamide dissolves neither cellulose nor lignocellulosic material.

Journal article

Niedermeyer H, Ab Rani MA, Lickiss PD, Hallett JP, Welton T, White AJP, Hunt PAet al., 2010, Understanding siloxane functionalised ionic liquids, Phys. Chem. Chem. Phys., Vol: 12, Pages: 2018-2029-2018-2029

Journal article

Welton T, 2009, Topics in Current Chemistry: Foreword, ISBN: 9783642017797

Book

Bini R, Chiappe C, Mestre VL, Pomelli CS, Welton Tet al., 2009, A theoretical study of the solvent effect on Diels-Alder reaction in room temperature ionic liquids using a supermolecular approach, THEORETICAL CHEMISTRY ACCOUNTS, Vol: 123, Pages: 347-352, ISSN: 1432-881X

Journal article

Wells TP, Hallett JP, Williams CK, Welton Tet al., 2009, ORGN 201-Esterification in ionic liquids: The influence of solvent basicity, ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, Vol: 237, ISSN: 0065-7727

Journal article

Hallett JP, Liotta CL, Ranieri G, Welton Tet al., 2009, Charge Screening in the S<sub>N</sub>2 Reaction of Charged Electrophiles and Charged Nucleophiles: An Ionic Liquid Effect, JOURNAL OF ORGANIC CHEMISTRY, Vol: 74, Pages: 1864-1868, ISSN: 0022-3263

Journal article

Hallett JP, Welton T, 2009, How polar are ionic liquids?, Pages: 33-38, ISSN: 1938-5862

Ionic liquids have recently become extremely popular solvents for a wide range of applications from electrochemistry to synthesis. From a solvation standpoint, ionic liquids are generally considered to be 'very polar' solvents. However, attempts to quantify the polarity of ionic liquids have yielded a confusing mixture of results - moderate dielectric constants, mixed solvatochromic parameters and adjustable water solubilities defy a simple classification of the polarity of ionic liquids. We attempt to clarify this confusing and conflicting picture by using the Kamlet-Taft polarity scales to shed light on the solution behaviour and explain how ionic liquids interact with a variety of solutes. Using these various parameters, different solution behaviours can be quantified and correlated, thus painting a descriptive picture of what 'polarity' means for an ionic solvent. ©The Electrochemical Society.

Conference paper

Hallett JP, Liotta CL, Ranieri G, Welton Tet al., 2009, In search of an "ionic liquid effect", Pages: 81-87, ISSN: 1938-5862

The application of liquids that are salts at room temperature to chemicals synthesis has become a hugely exciting field of study. Thousands of papers are now generated each year and several industrial chemicals processes are now running. The greatest promise that these ionic liquids hold is that they might offer process advantages, even novel behaviors that cannot be achieved in molecular solvents. However, until now no behavior that is unique to ionic liquids has been observed. For such an "ionic liquid effect" to be seen it would need to be the result of the medium being composed solely of ions in motion. We have been searching for an ionic liquid effect, which we can now report here, for most the last decade. We demonstrate that when two dissolved salts react with each other in ionic liquids they follow a fundamentally different pathway to when the same salts react in any molecular solvent. ©The Electrochemical Society.

Conference paper

Wells TP, Hallett JP, Williams CK, Welton Tet al., 2009, Esterification in ionic liquids: The influence of solvent basicity, Pages: 103-106, ISSN: 1938-5862

The rate of esterification is reported in a range of ionic and molecular solvents. The effects of solvent on esterification rate are examined by using a linear solvation energy relationship based on the Kamlet-Taft solvent polarity descriptors (α, β, and π*). It is shown that the basicity (β) of the solvent is the major factor in determining esterification rate and that the highest rates are observed in low basicity solvents. ©The Electrochemical Society.

Conference paper

Correia I, Welton T, 2009, An old reaction in new media: kinetic study of a platinum(II) substitution reaction in ionic liquids, DALTON TRANSACTIONS, Pages: 4115-4121, ISSN: 1477-9226

Journal article

Oromi-Farrus M, Eras J, Villorbina G, Torres M, Llopis-Mestre V, Welton T, Canela Ret al., 2008, [BMIM][PF<sub>6</sub>]Promotes the Synthesis of Halohydrin Esters from Diols Using Potassium Halides, ANALYTICAL SCIENCES, Vol: 24, Pages: 1341-1345, ISSN: 0910-6340

Journal article

Wells TP, Hallett JP, Williams CK, Welton Tet al., 2008, Esterification in ionic liquids: The influence of solvent basicity, JOURNAL OF ORGANIC CHEMISTRY, Vol: 73, Pages: 5585-5588, ISSN: 0022-3263

Journal article

Welton T, 2008, The sustainable chemist, MATERIALS TODAY, Vol: 11, Pages: 56-56, ISSN: 1369-7021

Journal article

Olivier-Bourbigou H, Vallée C, Welton T, Mehnert CP, Magna L, Dyson PJ, Zhao D, Brask J, Jørgensen CT, Kirk O, Bonnet P, McNulty Jet al., 2008, Catalysis in Nonaqueous Ionic Liquids (ILs): State-of-the-Art, Multiphase Homogeneous Catalysis, Pages: 413-546, ISBN: 9783527307210

Book chapter

Ranieri G, Hallett JP, Welton T, 2008, Nucleophilic reactions at cationic centers in ionic liquids and molecular solvents, INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, Vol: 47, Pages: 638-644, ISSN: 0888-5885

Journal article

Crosthwaite JM, Farmer VA, Hallett JR, Welton Tet al., 2008, Epoxidation of alkenes by Oxone<SUP>TM</SUP> using 2-alkyl-3, 4-dihydroisoquinolinium salts as catalysts in ionic liquids, JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, Vol: 279, Pages: 148-152, ISSN: 1381-1169

Journal article

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