dc.contributor.author |
Stasko, D |
en |
dc.contributor.author |
Hoffmann, SP |
en |
dc.contributor.author |
Kim, KC |
en |
dc.contributor.author |
Fackler, NLP |
en |
dc.contributor.author |
Larsen, AS |
en |
dc.contributor.author |
Drovetskaya, T |
en |
dc.contributor.author |
Tham, FS |
en |
dc.contributor.author |
Reed, CA |
en |
dc.contributor.author |
Rickard, Clifton |
en |
dc.contributor.author |
Boyd, Peter |
en |
dc.contributor.author |
Stoyanov, ES |
en |
dc.date.accessioned |
2011-09-12T04:03:40Z |
en |
dc.date.issued |
2002 |
en |
dc.identifier.citation |
Journal of the American Chemical Society 124(46):13869-13876 2002 |
en |
dc.identifier.issn |
0002-7863 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/7887 |
en |
dc.description.abstract |
Large, inert, weakly basic carborane anions of the icosahedral type CHB11R5X6- (R = H, Me; X = Cl, Br) allow ready isolation and structural characterization of discrete salts of the solvated proton, [H(solvent)x][CHB11R5X6], (solvent = common O-atom donor). These oxonium ion Brønsted acids are convenient reagents for the tuned delivery of protons to organic solvents with a specified number of donor solvent molecules and with acidities leveled to those of the chosen donor solvent. They have greater thermal stability than the popular [H(OEt2)2][BArF] acids based on fluorinated tetraphenylborate counterions because carborane anions can sustain much higher levels of acidity. When organic O-atom donors such as diethyl ether, tetrahydrofuran, benzophenone, and nitrobenzene are involved, the coordination number of the proton (x) in [H(solvent)x]+ is two. A mixed species involving the [H(H2O)(diethyl ether)]+ ion has also been isolated. These solid-state structures provide expectations for the predominant molecular structures of solvated protons in solution and take into account that water is an inevitable impurity in organic solvents. The O···O distances are all short, lying within the range from 2.35 to 2.48 Å. They are consistent with strong, linear O···H···O hydrogen bonding. Density functional theory calculations indicate that all H(solvent)2+ cations have low barriers to movement of the proton within an interval along the O···H···O trajectory, i.e., they are examples of so-called SSLB H-bonds (short, strong, low-barrier). Unusually broadened IR bands, diagnostic of SSLB H-bonds, are observed in these H(solvent)2+ cations. |
en |
dc.language |
EN |
en |
dc.relation.ispartofseries |
Journal of the American Chemical Society |
en |
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/0002-7863/ |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
en |
dc.subject |
WEAKLY COORDINATING ANIONS |
en |
dc.subject |
STRONG HYDROGEN-BOND |
en |
dc.subject |
CRYSTAL-STRUCTURE |
en |
dc.subject |
INFRARED-SPECTRA |
en |
dc.subject |
CARBORANE ANIONS |
en |
dc.subject |
SINGLE-CRYSTAL |
en |
dc.subject |
EXCESS PROTON |
en |
dc.subject |
HYDRONIUM ION |
en |
dc.subject |
MODEL SYSTEM |
en |
dc.subject |
IR-SPECTRA |
en |
dc.title |
Molecular structure of the solvated proton in isolated salts. Short, strong, low barrier (SSLB) H-bonds |
en |
dc.type |
Journal Article |
en |
dc.identifier.doi |
10.1021/ja012671i |
en |
pubs.issue |
46 |
en |
pubs.begin-page |
13869 |
en |
pubs.volume |
124 |
en |
dc.rights.holder |
Copyright: 2002 American Chemical Society |
en |
dc.identifier.pmid |
12431118 |
en |
pubs.end-page |
13876 |
en |
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
en |
pubs.subtype |
Article |
en |
pubs.elements-id |
5374 |
en |
pubs.org-id |
Science |
en |
pubs.org-id |
Chemistry |
en |
pubs.record-created-at-source-date |
2010-09-01 |
en |
pubs.dimensions-id |
12431118 |
en |