Zobrazeno 1 - 10
of 72
pro vyhledávání: '"J. Engwerda"'
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-7 (2020)
The feasibility of molecular assemblers as a device to control chemical reactions by positioning molecules with atomic precision is a matter of debate in the literature. Here the authors describe of a rudimentary synthetic molecular assembler, supram
Externí odkaz:
https://doaj.org/article/d6c579419c414cd38873d42fdd5400ea
Autor:
Sander J. T. Brugman, Anthonius H. J. Engwerda, Emma Kalkman, Erik de Ronde, Paul Tinnemans, Elias Vlieg
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 1, Pp 38-42 (2019)
The crystal structures of four dimethoxybenzaldehyde (C9H10O3) isomers, namely the 2,3-, 2,4-, 2,5- and 3,5- isomers, are reported and compared to the previously reported crystal structures of 3,4-dimethoxybenzaldehyde and 2,6-dimethoxybenzaldehyde.
Externí odkaz:
https://doaj.org/article/9ea4222e730645c2a7df70d2fbd23b19
A key goal of chemistry is to develop synthetic systems that mimic biology, such as self-assembling, self-replicating models of minimal life forms. Oscillations are often observed in complex biological networks, but oscillating, self-replicating spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81304baf49570c44f849232dc1fa0f27
https://ora.ox.ac.uk/objects/uuid:78830b53-98f2-4073-99f8-b326d38e6c11
https://ora.ox.ac.uk/objects/uuid:78830b53-98f2-4073-99f8-b326d38e6c11
Autor:
Mohammad Hossein Heydari, J. Engwerda, Ghasem Barid Loghmani, M. Saffarzadeh, Z. Nikooeinejad
Publikováno v:
Computational Economics. 59:775-801
In this article, we consider the impact uncertainty has on policies and realization of targets aimed at the stabilization of government debt. The problem is motivated by the fact that in many countries revenues are to a large extent uncertain. Follow
Autor:
Johannes A. A. W. Elemans, Kim H A van de Ven, Anouk Gasseling, Wester de Poel, Eleanor R. Townsend, Francesco Carlà, Willem J. P. van Enckevort, Ben L Werkhoven, James J. De Yoreo, Roberto Felici, Narendra M. Adhikari, Aashish Tuladhar, Sander J. T. Brugman, Maciej Jankowski, Jakub Drnec, Melian A. R. Blijlevens, Alan E. Rowan, Elias Vlieg, Anthonius H. J. Engwerda, Jordi de Lange
Publikováno v:
Angewandte Chemie. International Edition, 59, 6, pp. 2323-2327
Angewandte Chemie. International Edition, 59, 2323-2327
'Angewandte Chemie International Edition ', vol: 59, pages: 2323-2327 (2020)
Angewandte Chemie (International Ed. in English)
Angewandte Chemie. International Edition, 59, 2323-2327
'Angewandte Chemie International Edition ', vol: 59, pages: 2323-2327 (2020)
Angewandte Chemie (International Ed. in English)
Organothiol monolayers on metal substrates (Au, Ag, Cu) and their use in a wide variety of applications have been extensively studied. Here, the growth of layers of organothiols directly onto muscovite mica is demonstrated using a simple procedure. A
Autor:
E. de Ronde, Anthonius H. J. Engwerda, Emma Kalkman, Sander J. T. Brugman, Elias Vlieg, Paul Tinnemans
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 1, Pp 38-42 (2019)
Acta Crystallographica Section E-Crystallographic Communications, 75, 38
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E-Crystallographic Communications, 75, pp. 38
Acta Crystallographica Section E-Crystallographic Communications, 75, 38
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E-Crystallographic Communications, 75, pp. 38
The crystal structures of four dimethoxybenzaldehyde (C9H10O3) isomers are reported and compared to the previously reported crystal structures of 3,4-dimethoxybenzaldehyde and 2,6-dimethoxybenzaldehyde. All dimethoxybenzaldehy
Publikováno v:
Nature chemistry. 14(7)
A key goal of chemistry is to develop synthetic systems that mimic biology, such as self-assembling, self-replicating models of minimal life forms. Oscillations are often observed in complex biological networks, but oscillating, self-replicating spec
Autor:
Robert J. H. Scanes, Philipp Kukura, Josh Southworth, Stephen P. Fletcher, Maria A. Lebedeva, Anthonius H. J. Engwerda
Publikováno v:
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
Angewandte Chemie International Edition
We report chemically fuelled out‐of‐equilibrium self‐replicating vesicles based on surfactant formation. We studied the vesicles’ autocatalytic formation using UPLC to determine monomer concentration and interferometric scattering microscopy
Autor:
Kimberly M. Bonger, F. Matthias Bickelhaupt, Xian Riedijk, Selma Eising, Anthonius H. J. Engwerda
Publikováno v:
Bioconjugate Chemistry, 29, 9, pp. 3054-3059
Bioconjugate Chemistry, 29, 3054-3059
Bioconjugate Chemistry, 29, 3054-3059
Bioorthogonal reactions are selective transformations that are not affected by any biological functional group and are widely used for chemical modification of biomolecules. Recently, we reported that vinylboronic acids (VBAs) gave exceptionally high
Autor:
Floris P. J. T. Rutjes, Paul Tinnemans, Niels Koning, F. Matthias Bickelhaupt, Anthonius H. J. Engwerda, Hugo Meekes, Elias Vlieg
Publikováno v:
Crystal Growth & Design, 17, 8, pp. 4454-4457
Engwerda, A H J, Koning, N, Tinnemans, P, Meekes, H, Bickelhaupt, F M, Rutjes, F P J T & Vlieg, E 2017, ' Deracemization of a Racemic Allylic Sulfoxide Using Viedma Ripening ', Crystal Growth and Design, vol. 17, no. 8, pp. 4454-4457 . https://doi.org/10.1021/acs.cgd.7b00828
Crystal Growth & Design, 17, 4454-4457
Crystal Growth & Design
Crystal Growth and Design, 17(8), 4454-4457. American Chemical Society
Engwerda, A H J, Koning, N, Tinnemans, P, Meekes, H, Bickelhaupt, F M, Rutjes, F P J T & Vlieg, E 2017, ' Deracemization of a Racemic Allylic Sulfoxide Using Viedma Ripening ', Crystal Growth and Design, vol. 17, no. 8, pp. 4454-4457 . https://doi.org/10.1021/acs.cgd.7b00828
Crystal Growth & Design, 17, 4454-4457
Crystal Growth & Design
Crystal Growth and Design, 17(8), 4454-4457. American Chemical Society
Despite the importance of enantiopure chiral sulfoxides, few methods exist that allow for their deracemization. Here, we show that an enantiopure sulfoxide can be produced from the corresponding racemate using Viedma ripening involving rearrangement-