Zobrazeno 1 - 10
of 175
pro vyhledávání: '"Andreas W. Ehlers"'
Autor:
Devin H. A. Boom, Andreas W. Ehlers, Martin Nieger, Marc Devillard, Ghenwa Bouhadir, Didier Bourissou, J. Chris Slootweg
Publikováno v:
ACS Omega, Vol 3, Iss 4, Pp 3945-3951 (2018)
Externí odkaz:
https://doaj.org/article/a5da33d02c9a4b74863798808d872fba
Autor:
Ferry Heus, Reka A. Otvos, Ruud L. E. G. Aspers, Rene van Elk, Jenny I. Halff, Andreas W. Ehlers, Sébastien Dutertre, Richard J. Lewis, Sybren Wijmenga, August B. Smit, Wilfried M. A. Niessen, Jeroen Kool
Publikováno v:
Biology, Vol 3, Iss 1, Pp 139-156 (2014)
A nano-flow high-resolution screening platform, featuring a parallel chip-based microfluidic bioassay and mass spectrometry coupled to nano-liquid chromatography, was applied to screen animal venoms for nicotinic acetylcholine receptor like (nAChR) a
Externí odkaz:
https://doaj.org/article/dc6d540413ab4f87b51d13d1b61d298e
Autor:
Zhiyuan He, Lingyu Liu, Felix J. de Zwart, Xiaolian Xue, Andreas W. Ehlers, KaKing Yan, Serhiy Demeshko, Jarl Ivar van der Vlugt, Bas de Bruin, Jeremy Krogman
Publikováno v:
Inorganic Chemistry, 61(30), 11725-11733. American Chemical Society
In this paper we report the synthesis of a unique silicon(I)-based metalla-disilirane and report on its reactivity towards TMS-azide and benzophenone. Metal complexes containing disilylenes ((bis)silylenes with a Si‒Si bond) are known, but direct l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf7627cc3ade75caf5d62f764d51fda1
https://doi.org/10.1021/acs.inorgchem.2c01369
https://doi.org/10.1021/acs.inorgchem.2c01369
Autor:
Andreas W. Ehlers, Flip Holtrop, J. Chris Slootweg, Martin Nieger, Eduard O. Bobylev, Koop Lammertsma, Mark K. Rong
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Rong, M K, Holtrop, F, Bobylev, E O, Nieger, M, Ehlers, A W, Slootweg, J C & Lammertsma, K 2021, ' Atypical and Asymmetric 1,3-P,N Ligands : Synthesis, Coordination and Catalytic Performance of Cycloiminophosphanes ', Chemistry-A European Journal, vol. 27, no. 56, pp. 14007-14016 . https://doi.org/10.1002/chem.202101921
Chemistry-A European Journal, 27(56), 14007-14016. Wiley-VCH Verlag
Rong, M K, Holtrop, F, Bobylev, E O, Nieger, M, Ehlers, A W, Slootweg, J C & Lammertsma, K 2021, ' Atypical and Asymmetric 1,3-P,N Ligands : Synthesis, Coordination and Catalytic Performance of Cycloiminophosphanes ', Chemistry-A European Journal, vol. 27, no. 56, pp. 14007-14016 . https://doi.org/10.1002/chem.202101921
Chemistry-A European Journal, 27(56), 14007-14016. Wiley-VCH Verlag
Novel seven‐membered cyclic imine‐based 1,3‐P,N ligands were obtained by capturing a Beckmann nitrilium ion intermediate generated in situ from cyclohexanone with benzotriazole, and then displacing it by a secondary phosphane under triflic acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caf990e2f5b89ff36a13a6f19abac6aa
https://doi.org/10.1002/chem.202101921
https://doi.org/10.1002/chem.202101921
Publikováno v:
Chemphyschem
ChemPhysChem, 22(20), 2099-2106. Wiley-VCH Verlag
ChemPhysChem, 22(20), 2099-2106. Wiley-VCH Verlag
Supramolecular adducts between dimethyl‐2,2,3,3‐tetracyanocyclopropane (Me2TCCP) with 21 small (polar) molecules and 10 anions were computed with DFT (B3LYP‐D3/def2‐TZVP). Their optimized geometries were used to obtain interaction energies, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cf6bab216e71f4c01a8f136f714c22a
http://europepmc.org/articles/PMC8596889
http://europepmc.org/articles/PMC8596889
Autor:
Long Pham Ngoc, Andreas W. Ehlers, Eva de Rijke, Abraham Brouwer, Ha Dang Thi Cam, Bart van der Burg, Kees Swart, H.T. Besselink, Rick Helmus
Publikováno v:
Pham Ngoc, L, Helmus, R, Ehlers, A W, Swart, K, Besselink, H, De Rijke, E, Dang Thi Cam, H, Brouwer, A & Van Der Burg, B 2021, ' Effect-directed analysis and chemical identification of agonists of peroxisome proliferator-activated receptors in white button mushroom ', Food and Function, vol. 12, no. 1, pp. 133-143 . https://doi.org/10.1039/d0fo02071k
Food and Function, 12(1), 133-143. Royal Society of Chemistry
Food & Function
Food and Function, 12(1), 133-143. Royal Society of Chemistry
Food & Function
Obesity has a serious effect on human health. It relates to metabolic syndrome, including the associated disorders such as type 2 diabetes, heart disease, stroke and hyperemia. The peroxisome proliferator-activated receptors (PPARs) are important rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9de2ff1a776350fd21ec65dee8f575aa
http://www.scopus.com/inward/record.url?scp=85099594234&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85099594234&partnerID=8YFLogxK
Autor:
Flip Holtrop, Maximilian Paradiz Dominguez, Albert M. Brouwer, J. Chris Slootweg, René M. Williams, Bas de Bruin, Andreas W. Ehlers, Nicolaas P. van Leest, Andrew R. Jupp
Publikováno v:
Chemistry-A European Journal, 26(41), 9005-9011. Wiley-VCH Verlag
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry (Weinheim an Der Bergstrasse, Germany)
Archetypal phosphine/borane frustrated Lewis pairs (FLPs) are famed for their ability to activate small molecules. The mechanism is generally believed to involve two‐electron processes. However, the detection of radical intermediates indicates that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab5e4e32ef7019f154cf1797654b3bd4
https://doi.org/10.1002/chem.202001494
https://doi.org/10.1002/chem.202001494
Autor:
Emmanuel Nicolas, Andreas W. Ehlers, Andrew R. Jupp, Devin H. A. Boom, J. Chris Slootweg, Martin Nieger, Ewoud J. J. de Boed
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie, 646(13), 586-592. Wiley-VCH Verlag
The reaction of the intramolecular frustrated Lewis pair (FLP) tBu2PCH2BPh2 with the amine-boranes NH3 center dot BH3 and Me2NH center dot BH3 leads to the formation of the corresponding FLP-H2 adducts as well as novel five-membered heterocycles that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e0c5fb2237209abd664364e3031c32d
https://doi.org/10.1002/zaac.201900313
https://doi.org/10.1002/zaac.201900313
Autor:
Koop Lammertsma, Trevor A. Hamlin, Célia Fonseca Guerra, Andreas W. Ehlers, F. Matthias Bickelhaupt, Ayush K. Narsaria, Julian D. Ruijter
Publikováno v:
Journal of Computational Chemistry, 41(15), 1448-1455. John Wiley and Sons Inc.
Narsaria, A K, Ruijter, J D, Hamlin, T A, Ehlers, A W, Guerra, C F, Lammertsma, K & Bickelhaupt, F M 2020, ' Performance of TDDFT Vertical Excitation Energies of Core-Substituted Naphthalene Diimides ', Journal of Computational Chemistry, vol. 41, no. 15, pp. 1448-1455 . https://doi.org/10.1002/jcc.26188
Journal of Computational Chemistry
Journal of Computational Chemistry, 41, 15, pp. 1448-1455
Journal of Computational Chemistry, 41, 1448-1455
Narsaria, A K, Ruijter, J D, Hamlin, T A, Ehlers, A W, Guerra, C F, Lammertsma, K & Bickelhaupt, F M 2020, ' Performance of TDDFT Vertical Excitation Energies of Core-Substituted Naphthalene Diimides ', Journal of Computational Chemistry, vol. 41, no. 15, pp. 1448-1455 . https://doi.org/10.1002/jcc.26188
Journal of Computational Chemistry
Journal of Computational Chemistry, 41, 15, pp. 1448-1455
Journal of Computational Chemistry, 41, 1448-1455
We have evaluated the performance of various density functionals, covering generalized gradient approximation (GGA), global hybrid (GH) and range‐separated hybrid (RSH), using time dependent density functional theory (TDDFT) for computing vertical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7e93098301e0ce0543e18b748e497e3
https://doi.org/10.1002/jcc.26188
https://doi.org/10.1002/jcc.26188
Autor:
Koop Lammertsma, J. Chris Slootweg, Martin Nieger, Maximilian Joost, Martin Lutz, Andreas W. Ehlers
Publikováno v:
Joost, M, Nieger, M, Lutz, M, Ehlers, A W, Slootweg, J C & Lammertsma, K 2020, ' Synthesis, Structures, and Electronic Properties of O-And S-Heterocyclic Carbene Complexes of Iridium, Copper, Silver, and Gold ', Organometallics, vol. 39, no. 10, pp. 1762-1771 . https://doi.org/10.1021/acs.organomet.0c00066
Organometallics, 39(10), 1762-1771. American Chemical Society
Organometallics, 39(10), 1762. American Chemical Society
Organometallics, 39(10), 1762-1771. American Chemical Society
Organometallics, 39(10), 1762. American Chemical Society
O- and S-heterocyclic carbenes (OHCs, SHCs) are shown experimentally and computationally to be stronger pi acceptors than NHCs and lack, of course, substituents at the heteroatoms. These different electronic and steric characteristics make OHCs and S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6916ec57ade1012566c47f9791cdbd86
http://www.scopus.com/inward/record.url?scp=85085947272&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85085947272&partnerID=8YFLogxK