Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jonas Altnöder"'
Publikováno v:
Angewandte Chemie. 128:1955-1959
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57e1ab3a8603012698c22e911f89dcff
https://doi.org/10.1002/ange.201508481
https://doi.org/10.1002/ange.201508481
Publikováno v:
Journal of Molecular Structure
Journal of Molecular Structure, Elsevier, 2014, 1076, pp.344-351. ⟨10.1016/j.molstruc.2014.07.061⟩
Journal of Molecular Structure, Elsevier, 2014, 1076, pp.344-351. ⟨10.1016/j.molstruc.2014.07.061⟩
The effect of hydration on a flexible amphiphilic molecule has been studied on the example of 1-hydroxyindan (1-indanol). Studies in jet-cooled conditions by means of resonance-enhanced two-photon ionization and IR–UV double resonance experiments s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ef042be114dcdf182424232936f40fa
https://doi.org/10.1016/j.molstruc.2014.07.061
https://doi.org/10.1016/j.molstruc.2014.07.061
Autor:
Fabian Hecker, Dmitriy Borodin, Marcel Levien, Kerstin Krüger, Marco Eckhoff, Xuan T. Nguyen, Darius Rohleder, Martin A. Suhm, Jonas Altnöder, Lennart Reuter, Helen Preiß, Roland A. Schulz
Publikováno v:
The Chemical Record. 14:1116-1133
A systematic review and analysis of the most stable spatial arrangements of n carbon, n oxygen, and 2n hydrogen atoms including vibrational zero-point energy up to n = 5 shows that small-molecule aggregates win, typically followed by thermally unstab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bee35e67f7e2acf08e29141e68893139
https://doi.org/10.1002/tcr.201402059
https://doi.org/10.1002/tcr.201402059
Autor:
Melanie Schnell, Fabian Dietrich, Jonas Altnöder, Martin A. Suhm, Markus Gerhards, Sabrina Zinn, Matthias Heger, Anke Stamm, Anja Poblotzki, Chris Medcraft, Dominic Bernhard
Publikováno v:
Physical Chemistry Chemical Physics
Physical chemistry, chemical physics 18(37), 25975-25983 (2016). doi:10.1039/C6CP03557D
Physical chemistry, chemical physics 18(37), 25975-25983 (2016). doi:10.1039/C6CP03557D
Dispersion interactions are omnipresent in intermolecular interactions, but their respective contributions are difficult to predict. Aromatic ethers offer competing docking sites for alcohols: the ether oxygen as a well known hydrogen bond acceptor,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c69bbc475a0745b24785dedbb58f9f0
https://hdl.handle.net/11858/00-001M-0000-002B-8115-1
https://hdl.handle.net/11858/00-001M-0000-002B-8115-1
Methanol is shown to engage two nearly equivalent solvation sites in 2,5-dimethylfuran, the electronrich p cloud and the electron-deficient oxygen site. The latter only wins by a slight margin, thanks to the methyl group undergoing secondary interact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aba82bbf6310a07a009c46cc490429a
http://resolver.sub.uni-goettingen.de/purl?gs-1/13716
http://resolver.sub.uni-goettingen.de/purl?gs-1/13716
Anisole offers two similarly attractive hydrogen bond acceptor sites to an incoming hydrogen bond donor: its oxygen atom and its delocalized π electron system. Electronic structure calculations up to the CCSD(T)/AVTZ level suggest an isoenergetic si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcdbd4f8230a5b6777599ef1a8c5650d
http://resolver.sub.uni-goettingen.de/purl?gs-1/11810
http://resolver.sub.uni-goettingen.de/purl?gs-1/11810
Autor:
Jonas, Altnöder, Kerstin, Krüger, Dmitriy, Borodin, Lennart, Reuter, Darius, Rohleder, Fabian, Hecker, Roland A, Schulz, Xuan T, Nguyen, Helen, Preiß, Marco, Eckhoff, Marcel, Levien, Martin A, Suhm
Publikováno v:
Chemical record (New York, N.Y.). 14(6)
A systematic review and analysis of the most stable spatial arrangements of n carbon, n oxygen, and 2n hydrogen atoms including vibrational zero-point energy up to n = 5 shows that small-molecule aggregates win, typically followed by thermally unstab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e23e10009de72d30babada1c3c5d9f99
https://pubmed.ncbi.nlm.nih.gov/25316264
https://pubmed.ncbi.nlm.nih.gov/25316264
Publikováno v:
The journal of physical chemistry. A. 118(18)
The monomers and hydrogen-bonded dimers of benzyl alcohol, cyclohexylmethanol, and 2-methyl-1-propanol are investigated by jet-FTIR spectroscopy, complemented by Raman spectra and quantum chemical calulations, including CCSD(T) corrections. A large v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6042af6cdcf06920e57f030c7916fd8f
https://pubmed.ncbi.nlm.nih.gov/24758292
https://pubmed.ncbi.nlm.nih.gov/24758292
Autor:
Aude Bouchet, Jonas Altnöder, Juhyon J. Lee, Anne Zehnacker-Rentien, Katharina E. Otto, Martin A. Suhm
Publikováno v:
Physical chemistry chemical physics : PCCP. 15(25)
The aggregation behavior of racemic and enantiopure 1-indanol has been studied by FTIR spectroscopy, resonant ion dip IR spectroscopy, and spontaneous Raman scattering in supersonic jets. This triple experimental approach, augmented by homology to re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d95cd51c1ea79e6efb28589c8256a588
https://pubmed.ncbi.nlm.nih.gov/23665542
https://pubmed.ncbi.nlm.nih.gov/23665542
Publikováno v:
ChemistryOpen
Carbohydrates are used in nature as molecular recognition tools. Understanding their conformational behavior upon aggregation helps in rationalizing the way in which cells and bacteria use sugars to communicate. Here, the simplest α-hydroxy carbonyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da0f2d98a74aa022a8efc79cebe65083
https://pubmed.ncbi.nlm.nih.gov/24551516
https://pubmed.ncbi.nlm.nih.gov/24551516