Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Orion B. Berryman"'
Anion Influence on the Packing of 1,3-Bis(4-Ethynyl-3-Iodopyridinium)-Benzene Halogen Bond Receptors
Publikováno v:
Crystals, Vol 9, Iss 10, p 522 (2019)
Rigid and directional arylethynyl scaffolds have been widely successful across diverse areas of chemistry. Utilizing this platform, we present three new structures of a dicationic 1,3-bis(4-ethynyl-3-iodopyridinium)-benzene halogen bonding receptor w
Externí odkaz:
https://doaj.org/article/0e38cedca3834d11bd1846ab83f73ac1
Autor:
Daniel A. Decato, Orion B. Berryman
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 9, Pp o667-o668 (2015)
The asymmetric unit of the title compound, C21H14O6, comprises two symmetrically independent molecules that form a locally centrosymmetric hydrogen-bonded dimer, with the planes of the corresponding carboxylic acid groups rotated by 15.8 (1) and 17.5
Externí odkaz:
https://doaj.org/article/3862535cd719460eb96a412d0b147f66
Publikováno v:
Chemical Science. 13:11156-11162
C-H hydrogen bonds have remarkable impacts on various chemical systems. Here we consider the influence of C-H hydrogen bonds to iodine atoms. Positioning a methyl group between two iodine halogen bond donors of the receptor engendered intramolecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e8fd76edfd7de2d3437befe76184f23
https://doi.org/10.1039/d2sc03792k
https://doi.org/10.1039/d2sc03792k
Autor:
Flóra Boróka Németh, Máté Erdélyi, Lotta Turunen, Orion B. Berryman, Imre Pápai, Daniel A. Decato
Publikováno v:
Bulletin of the Chemical Society of Japan. 94:191-196
A distinct difference between the three-center halogen bond and the analogous three-center coordinative bond of silver is demonstrated by computational, X-ray crystallographic and solution NMR spec...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b323a0d24df8b90793aa8246b95feef2
https://doi.org/10.1246/bcsj.20200274
https://doi.org/10.1246/bcsj.20200274
Publikováno v:
Halogen Bonding in Solution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0de56bdc5d46b87978067b2f7f8c0fc7
https://doi.org/10.1002/9783527825738.ch1
https://doi.org/10.1002/9783527825738.ch1
Autor:
Daniel A. Decato, Orion B. Berryman, James H. May, Vyacheslav S. Bryantsev, Asia Marie S. Riel
Publikováno v:
Angew Chem Int Ed Engl
Proximal noncovalent forces are commonplace in natural systems and understanding the consequences of their juxtaposition is critical. This paper experimentally quantifies for the first time a Hydrogen Bond enhanced Halogen Bond (HBeXB) without the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60b914f39a052e5998ee9f39d94078f6
https://doi.org/10.1002/ange.202012262
https://doi.org/10.1002/ange.202012262
Publikováno v:
Chem Rev
Using anions to induce molecular structure is a rapidly growing area of dynamic and switchable supramolecular chemistry. The emphasis of this review is on helical anion foldamers in solution, and many of the beautiful complexes described herein are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb22fe32fb768e34e2ea911f47139f4e
https://doi.org/10.1021/acs.chemrev.9b00583
https://doi.org/10.1021/acs.chemrev.9b00583
Publikováno v:
Chem Commun (Camb)
Recent results indicate a halogen bond donor is strengthened through direct interaction with a hydrogen bond to the electron-rich belt of the halogen. Here, this Hydrogen Bond enhanced Halogen Bond (HBeXB) plays a clear role in a catalyst. Our HBeXB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcfde20b16e3171f07f078d460e67bae
https://europepmc.org/articles/PMC8919959/
https://europepmc.org/articles/PMC8919959/
Publikováno v:
Cryst Growth Des
A family of pyridyl-functionalized arylacetylene C–H hydrogen bonding (HB) receptors were synthesized and binding interactions to perrhenate (ReO4–) studied in the solid state. The protonation and alkylation state of the pyridine nitrogen dictate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6701cc8e7d8f01988e5f45f623eff6c6
https://pubmed.ncbi.nlm.nih.gov/34163307
https://pubmed.ncbi.nlm.nih.gov/34163307
The behavior of an enediyne photoswitch is modulated with halogen bonding, coordinative bonding and hydrogen bonding. Through NMR and computational studies we demonstrate that the relative strength of the secondary bonding directly influences the rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1d0598a1e05276d892d4cde0c185479
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-448937
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-448937