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@ARTICLE{Bator:18307,
author = {Bator, G. and Sawka-Dobrowolska, W. and Sobczyk, L. and
Grech, E. and Nowicka-Scheibe, J. and Pawlukojc, A. and
Wuttke, J. and Baran, J. and Owczarek, M.},
title = {4,4'-, 5,5'- and 6,6' -dimethyl-2,2'-bipyridyls: the
structures, phase transitions, vibrations and methyl group
tunneling of their complexes with chloranilic acid},
journal = {The journal of chemical physics},
volume = {135},
issn = {0021-9606},
address = {Melville, NY},
publisher = {American Institute of Physics},
reportid = {PreJuSER-18307},
pages = {044509},
year = {2011},
note = {This work was supported by the Polish Ministry of Science
and Higher Education (Project Register No. N N204 2497 34)
and partially by the International Programme ZIBJ DUBNA
04-4-1069-2009/2010.04.29 (Decision No. 868/W-ZIBJ
DUBNA/2010/0). This research project has been supported by
the European Commission under the 7th Framework Programme
through the Key Action: Strengthening the European Research
Area, Research Infrastructures (Contract No. 226507
(NMI3)).},
abstract = {The crystal and molecular structures of 4,4(')- and
6,6(')-dimethyl-2,2(')-bipyridyl complexes with
2,5-dichloro-3,6-dihydroxy-p-benzoquinone (chloranilic acid,
CLA) have been determined and compared with those of the
complex with the 5,5(')-derivative, which is known to
possess interesting antiferroelectric properties. In the
crystalline state, all three compounds form hydrogen bonded
chains with N(+)-H···O(-) and O-H···N bridges on both
sides of the bipyridyl constituent. The comparison of three
derivatives indicates that the N(+)-H···O(-) hydrogen
bonds are shortest for the 5,5(')-dimethyl complex. The
4,4(')- and 6,6(')-derivatives do not show any ferroelectric
feature. The 6,6(')-one is, however, characterized by a
continuous phase transition, revealed in the differential
scanning calorimetry, dilatometric, and dielectric
characteristics. The tunneling splitting measured by neutron
backscattering in the energy range ±30 μeV for the neat
dimethyl bipyridyls and their complexes with CLA indicates
that the different splittings are primarily due to the
crystal packing effect and that charge transfer between
interacting compounds plays only a minor role.},
keywords = {J (WoSType)},
cin = {ICS-1 / JCNS-FRM-II (JCNS (München) ; Jülich Centre for
Neutron Science JCNS (München) ; JCNS-FRM-II) / JCNS-1 /
JCNS-2},
ddc = {540},
cid = {I:(DE-Juel1)ICS-1-20110106 /
I:(DE-Juel1)JCNS-FRM-II-20110218 /
I:(DE-Juel1)JCNS-1-20110106 / I:(DE-Juel1)JCNS-2-20110106},
pnm = {BioSoft: Makromolekulare Systeme und biologische
Informationsverarbeitung / Großgeräte für die Forschung
mit Photonen, Neutronen und Ionen (PNI)},
pid = {G:(DE-Juel1)FUEK505 / G:(DE-Juel1)FUEK415},
experiment = {EXP:(DE-MLZ)SPHERES-20140101},
shelfmark = {Physics, Atomic, Molecular $\&$ Chemical},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:21806140},
UT = {WOS:000293477300058},
doi = {10.1063/1.3613640},
url = {https://juser.fz-juelich.de/record/18307},
}