Corrosion inhibition in acidic environments: key interfacial insights with photoelectron spectroscopy

Autor: Kiran Kousar, Michael Dowhyj, Monika S. Walczak, Thomas Ljungdahl, Alexander Wetzel, Hans Oskarsson, Alex S. Walton, Paolo Restuccia, Nicholas M. Harrison, Robert Lindsay

Publikováno v: Kousar, K, Dowhyj, M, Walczak, M, Ljungdahl, T, Wetzel, A, Oskarsson, H, Walton, A, Restuccia, P, Harrison, N & Lindsay, R 2022, ' Corrosion Inhibition in Acidic Environments: Key Interfacial Insights with Photoelectron Spectroscopy ', Faraday Discussions . https://doi.org/10.1039/D1FD00106J

In many engineering scenarios, surface-active organic species are added to acidic solutions to inhibit the corrosion of metallic components. Given suitable selection, such corrosion inhibitors are highly effective, preventing significant degradation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f94ce7b0d56aad6bb270719d9ccaa9d
https://pubmed.ncbi.nlm.nih.gov/35506395

Propoxylation of fatty amines: Switching from batch to flow

Autor: Pia Müller, John van der Schaaf, Thomas Ljungdahl, Alejo Aguirre

Publikováno v: Journal of Advanced Manufacturing and Processing. 2

The ethoxylation and propoxylation of fatty amines are important industrial reactions commonly performed in de‐intensified semi‐batch reactors. The present study aims to intensify these reactions by transferring the process to continuous processi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85265dee9123b7364e2d10e97da83d3b
https://doi.org/10.1002/amp2.10042

Solid-Phase Synthesis of 5′-O-[N-(Acyl)sulfamoyl]adenosine Derivatives

Autor: Hanna Jacobson Ingemyr, Christopher P. Lawson, Thomas Ljungdahl, Itedale Namro Redwan, Morten Grøtli

Publikováno v: European Journal of Organic Chemistry. 2012:3665-3669

The solid-phase synthesis of 5'-O-[N-(acyl)sulfamoyl]adenosine derivatives is described. The use of a Rink amide polystyrene solid support together with an appropriately protected ribo-purine starting material allowed for the development of a highly

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https://doi.org/10.1002/ejoc.201200329

Positional Scanning Peptide Libraries for Kinase Substrate Specificity Determinations: Straightforward and Reproducible Synthesis Using Pentafluorophenyl Esters

Autor: Morten Grøtli, Jenny Veide-Vilg, Thomas Ljungdahl, Fredrik K. Wallner, Markus J. Tamás

Publikováno v: Journal of Combinatorial Chemistry. 12:733-742

An efficient method to synthesize positional scanning synthetic combinatorial libraries (PS-SCLs) for studying the specificity of protein kinases is presented. Isokinetic ratios for pentafluorophenyl esters were determined iteratively using a new app

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3fd932dc9de367a7c6516f595ce8843
https://doi.org/10.1021/cc100095y

Two Competing Mechanisms for the Copper-Free Sonogashira Cross-Coupling Reaction

Autor: Thomas Ljungdahl, Hans Emtenäs, Jerker Mårtensson, T.H Bennur, Andrea Dallas

Publikováno v: Organometallics. 27:2490-2498

The mechanism of the copper-free Sonogashira cross-coupling was investigated using a model reaction with differently para-substituted phenylacetylenes and 4-iodobenzotrifluoride as coupling partners and a Pd2(dba)3·CHCl3−AsPh3 catalyst system in m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9706066a030ec9920b9f47e49ebb6b55
https://doi.org/10.1021/om800251s