Chalcogen Bonds: How to Characterize Them in Solution?
IR spectroscopy
ITC
Mmultinuclear NMR
UV-visible spectroscopy
chalcogen bond
Journal
Chemphyschem : a European journal of chemical physics and physical chemistry
ISSN: 1439-7641
Titre abrégé: Chemphyschem
Pays: Germany
ID NLM: 100954211
Informations de publication
Date de publication:
14 Feb 2023
14 Feb 2023
Historique:
revised:
07
10
2022
received:
07
07
2022
pubmed:
8
10
2022
medline:
8
10
2022
entrez:
7
10
2022
Statut:
ppublish
Résumé
Chalcogen bonds (ChBs) occur between molecules containing Lewis acidic chalcogen substituents and Lewis bases. Recently, ChB emerged as a pivotal interaction in solution-based applications such as anion recognition, anion transport and catalysis. However, before moving to applications, the involvement of ChB must be established in solution. In this Concept article, we provide a brief review of the currently available experimental investigations of ChB in solution.
Identifiants
pubmed: 36205925
doi: 10.1002/cphc.202200481
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202200481Subventions
Organisme : University of Strasbourg
Organisme : CNRS
Organisme : French National Research Agency
ID : ANR-21-CE07-0014
Informations de copyright
© 2022 The Authors. ChemPhysChem published by Wiley-VCH GmbH.
Références
C. B. Aakeroy, D. L. Bryce, G. R. Desiraju, A. Frontera, A. C. Legon, F. Nicotra, K. Rissanen, S. Scheiner, G. Terraneo, P. Metrangolo, G. Resnati, Pure Appl. Chem. 2019, 91, 1889-1892.
J. S. Murray, P. Lane, T. Clark, P. Politzer, J. Mol. Model. 2007, 13, 1033-1038.
P. Politzer, J. S. Murray, ChemPhysChem 2020, 21, 579-588.
T. Clark, M. Hennemann, J. S. Murray, P. Politzer, J. Mol. Model. 2007, 13, 291-296.
J. M. Holthoff, E. Engelage, R. Weiss, S. M. Huber, Angew. Chem. Int. Ed. 2020, 59, 11150-11157;
Angew. Chem. 2020, 132, 11244-11251;
D. J. Pascoe, K. B. Ling, S. L. Cockroft, J. Am. Chem. Soc. 2017, 139, 15160-15167;
V. Oliveira, D. Cremer, E. Kraka, J. Phys. Chem. A 2017, 121, 6845-6862;
L. de Azevedo Santos, S. C. C. van der Lubbe, T. A. Hamlin, T. C. Ramalho, F. M. Bickelhaupt, ChemistryOpen 2021, 10, 391-401.
G. Cavallo, P. Metrangolo, R. Milani, T. Pilati, A. Priimagi, G. Resnati, G. Terraneo, Chem. Rev. 2016, 116, 2478-2601.
R. Weiss, E. Aubert, P. Pale, V. Mamane, Angew. Chem. Int. Ed. 2021, 60, 19281-19286.
S. Kolb, G. A. Oliver, D. B. Werz, Angew. Chem. Int. Ed. 2020, 59, 22306-22310;
Angew. Chem. 2020, 132, 22490-22495.
P. Scilabra, G. Terraneo, G. Resnati, Acc. Chem. Res. 2019, 52, 1313-1324.
M. Iwaoka, S. Takemoto, S. Tomoda, J. Am. Chem. Soc. 2002, 124, 10613-10620;
B. R. Beno, K.-S. Yeung, M. D. Bartberger, L. D. Pennington, N. A. Meanwell, J. Med. Chem. 2015, 58, 4383-4438;
K. Kříž, J. Fanfrlík, M. Lepšík, ChemPhysChem 2018, 19, 2540-2548.
K. T. Mahmudov, A. V. Gurbanov, V. A. Aliyeva, M. F. C. Guedes da Silva, G. Resnati, A. J. L. Pombeiro, Coord. Chem. Rev. 2022, 464, 214556.
N. Biot, D. Bonifazi, Coord. Chem. Rev. 2020, 413, 213243;
G. E. Garrett, E. I. Carrera, D. S. Seferos, M. S. Taylor, Chem. Commun. 2016, 52, 9881-9884;
S. Benz, M. Macchione, Q. Verolet, J. Mareda, N. Sakai, S. Matile, J. Am. Chem. Soc. 2016, 138, 9093-9096;
S. Benz, J. López-Andarias, J. Mareda, N. Sakai, S. Matile, Angew. Chem. Int. Ed. 2017, 56, 812-815;
Angew. Chem. 2017, 129, 830-833.
R. Weiss, E. Aubert, L. Groslambert, P. Pale, V. Mamane, Chem. Eur. J. 2022, 28, e202200395.
A. Bauzá, I. Alkorta, A. Frontera, J. Elguero, J. Chem. Theory Comput. 2013, 9, 5201-5210;
N. Mehta, T. Fellowes, J. M. White, L. Goerigk, J. Chem. Theory Comput. 2021, 17, 2783-2806.
V. Jurásková, F. Célerse, R. Laplaza, C. Corminboeuf, J. Chem. Phys. 2022, 156, 154112.
A. Elmi, S. L. Cockroft, Acc. Chem. Res. 2021, 54, 92-103.
Y. Nagao, T. Hirata, S. Goto, S. Sano, A. Kakehi, K. Iizuka, M. Shiro, J. Am. Chem. Soc. 1998, 120, 3104-3110.
J. Lu, Y. Lu, S. Yang, W. Zhu, Struct. Chem. 2011, 22, 757-763.
C. M. Young, A. Elmi, D. J. Pascoe, R. K. Morris, C. McLaughlin, A. M. Woods, A. B. Frost, A. de la Houpliere, K. B. Ling, T. K. Smith, A. M. Z. Slawin, P. H. Willoughby, S. L. Cockroft, A. D. Smith, Angew. Chem. Int. Ed. 2020, 59, 3705-3710;
Angew. Chem. 2020, 132, 3734-3739.
M. Iwaoka, H. Komatsu, T. Katsuda, S. Tomoda, J. Am. Chem. Soc. 2004, 126, 5309-5317.
X. He, X. Wang, Y.-L. Tse, Z. Ke, Y.-Y. Yeung, Angew. Chem. Int. Ed. 2018, 57, 12869-12873;
Angew. Chem. 2018, 130, 13051-13055.
R. Zeng, Z. Gong, Q. Yan, J. Org. Chem. 2020, 85, 8397-8404.
S. M. Walter, F. Kniep, L. Rout, F. P. Schmidtchen, E. Herdt-weck, S. M. Huber, J. Am. Chem. Soc. 2012, 134, 8507-8512.
P. Wonner, A. Dreger, L. Vogel, E. Engelage, S. M. Huber, Angew. Chem. Int. Ed. 2019, 58, 16923-16927;
Angew. Chem. 2019, 131, 17079-17083.
A. Borissov, I. Marques, J. Y. C. Lim, V. Félix, M. D. Smith, P. D. Beer, J. Am. Chem. Soc. 2019, 141, 4119-4129.
L. Chen, J. Xiang, Y. Zhao, Q. Yan, J. Am. Chem. Soc. 2018, 140, 7079-7082;
R. Zeng, Z. Gong, L. Chen, Q. Yan, ACS Macro Lett. 2020, 9, 1102-1107.
G. E. Garrett, G. L. Gibson, R. N. Straus, D. S. Seferos, M. S. Taylor, J. Am. Chem. Soc. 2015, 137, 4126-4133.
S. Benz, J. Mareda, C. Besnard, N. Sakai, S. Matile, Chem. Sci. 2017, 8, 8164-8169.
K. Strakova, L. Assies, A. Goujon, F. Piazzolla, H. V. Humeniuk, S. Matile, Chem. Rev. 2019, 119, 10977-11005.
L. Cui, Y. Gong, X. Yu, C. Lv, X. Du, J. Zhao, Y. Che, ACS Sens. 2021, 6, 2851-2857.
Y. Geboes, F. De Vleeschouwer, F. De Proft, W. A. Herrebout, Chem. Eur. J. 2017, 23, 17384-17392.
Y. Geboes, E. De Vos, W. A. Herrebout, New J. Chem. 2018, 42, 10563-10571.