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@ARTICLE{Ahmed:112080,
author = {Ahmed, M. and Ganesan, A. and Wang, F. and Feyer, V. and
Plekan, O. and Prince, K. C.},
title = {{P}hotoelectron {S}pectra of {S}ome {A}ntibiotic {B}uilding
{B}locks: 2-{A}zetidinone and {T}hiazolidine-{C}arboxylic
{A}cid},
journal = {The journal of physical chemistry $\<Washington,$ $DC\>$ /
A},
volume = {116},
issn = {1089-5639},
address = {Washington, DC},
publisher = {Soc.},
reportid = {PreJuSER-112080},
pages = {8653 - 8660},
year = {2012},
note = {We wish to thank Professor D. P. Chong for his assistance
in the Delta DFT calculations. M.A. and A.G. acknowledge the
Swinburne University Postgraduate Research Award (SUPRA) and
the Australian Research Council (ARC) for scholarship
support. The National Computational Infrastructure (NCI) at
the Australian National University under the Merit
Allocation Scheme (MAS), the Victorian Partnership for
Advanced Computing (VPAC), and Swinburne University
Supercomputing Facilities are acknowledged. We acknowledge
the Australian Synchrotron for travel funding under the
International Synchrotron Access Program (ISAP) and
Sincrotrone Trieste (Elettra) for beamtime allocation. We
thank our colleagues at Elettra for providing good quality
synchrotron light.},
abstract = {X-ray photoelectron spectra of the core and valence levels
of the fundamental building blocks of β-lactam antibiotics
have been investigated and compared with theoretical
calculations. The spectra of the compounds 2-azetidinone and
the 2- and 4-isomers of thiazolidine-carboxylic acid are
interpreted in the light of theoretical calculations. The
spectra of the two isomers of thiazolidine-carboxylic acid
are rather similar, as expected, but show clear effects due
to isomerization. Both isomers are analogues of proline,
which is well-known to populate several low energy
conformers in the gas phase. We have investigated the low
energy conformers of thiazolidine-4-carboxylic acid
theoretically in more detail and find some spectroscopic
evidence that multiple conformers may be present. The
measured valence levels are assigned for all three
compounds, and the character of the frontier orbitals is
identified and analyzed.},
keywords = {J (WoSType)},
cin = {PGI-6},
ddc = {530},
cid = {I:(DE-Juel1)PGI-6-20110106},
pnm = {Grundlagen für zukünftige Informationstechnologien},
pid = {G:(DE-Juel1)FUEK412},
shelfmark = {Chemistry, Physical / Physics, Atomic, Molecular $\&$
Chemical},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:22799571},
UT = {WOS:000307749000027},
doi = {10.1021/jp302950y},
url = {https://juser.fz-juelich.de/record/112080},
}