Vera Hamplova

Dr. Vera Hamplova

orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 July 1999 in Physical Review E
Verified
Journal Article
Closed access
PDF file
FGFrank Giesselmann
Frank Giesselmann
PZP. Zugenmaier
P. Zugenmaier
IDI. Dierking
I. Dierking
SLS. T. Lagerwall
S. T. Lagerwall
BSB. Stebler
B. Stebler
MGM. Glogarová
M. Glogarová
The smectic layer spacing of a nonfluorinated ferroelectric liquid crystal (FLC) compound with almost no shrinkage and only minor tendency to form zigzag defects was characterized by small angle x-ray diffraction. The material lacks a nematic phase. The smectic-A*–smectic-C* phase transition was studied by measuring the thermal and electric field response of the optical tilt and the electric polarization. These properties are described very well by a Landau expansion even without introduction of a higher-order Θ6 term. This result suggests a pure second-order phase transition far from tricriticality and differs considerably from the typical behavior of the A*−C* transition in most FLC materials.

1 December 2008 in Journal of Molecular Structure
Verified
Journal Article
Closed access
Alexej BubnovAlexej Bubnov
Alexej Bubnov
VNVladimira Novotna
Vladimira Novotna
VHVera Hamplova
Vera Hamplova
MKMiroslav Kašpar
Miroslav Kašpar
MGMilada Glogarová
Milada Glogarová

1 August 1996 in Chemical Physics Letters
Verified
Journal Article
Closed access
KNK. Nitsch
K. Nitsch
VHVera Hamplova
Vera Hamplova
MNMartin Nikl
Martin Nikl
KPK. Polák
K. Polák
MRM. Rodová
M. Rodová

27 April 2016 in Journal of Materials Chemistry C
Verified
Journal Article
Closed access
PDF file
MCMartin Cigl
Martin Cigl
Alexej BubnovAlexej Bubnov
Alexej Bubnov
MKMiroslav Kašpar
Miroslav Kašpar
FHFrantišek Hampl
František Hampl
VHVera Hamplova
Vera Hamplova
JSJiří Svoboda
Jiří Svoboda
Novel azobenzene-based photosensitive mesogens with lactate chiral units were synthesized. In order to modify the rate of the thermal Z–E isomerization of these compounds, small lateral substituents were introduced into their core in the proximity of the azo group. The influence of lateral substitution on the kinetics of the Z–E isomerization, mesomorphic behaviour, and UV-Vis absorption spectra was studied. It was found that the position of the substituents in the azobenzene core significantly affects the rate of their thermal isomerization. The stability of Z-isomers of several studied compounds is comparable to that of compounds with complex molecular structures designed for optical data storage. Although lateral substitution influences the breadth/length ratio of the core, liquid-crystalline properties of the studied materials have been preserved.

1 August 2001 in Liquid Crystals
Verified
Journal Article
Closed access
MKM. Ka[Sbreve]Par
M. Ka[Sbreve]Par
VHVera Hamplova
Vera Hamplova
VNVladimira Novotna
Vladimira Novotna
MGM. Glogarová
M. Glogarová
DPDamian Pociecha
Damian Pociecha
PVP. Van[Ebreve]K
P. Van[Ebreve]K
New series of liquid crystals with a chiral chain containing two asymmetric carbon atoms in two lactate groups have been synthesized. Some compounds have a third asymmetric centre in an (S)-2-methylbutyl alkyl chain. All the new compounds have SmA, SmC* and hexatic phases. Two of the homologues with three chiral centres also exhibit very wide SmCA phases and one of them a re-entrant SmC* phase. The phases are characterized by DSC, dielectric, and X-ray studies. Spontaneous polarization and tilt angle are determined for the polar phases.

19 January 2016 in RSC Advances
Verified
Journal Article
Closed access
PDF file
Alexej BubnovAlexej Bubnov
Alexej Bubnov
AIAgnieszka Iwan
Agnieszka Iwan
MCMartin Cigl
Martin Cigl
BBBartosz Boharewicz
Bartosz Boharewicz
ITIgor Tazbir
Igor Tazbir
VHVera Hamplova
Vera Hamplova
New photosensitive liquid crystalline compounds with a specific molecular structure have been designed in order to use them as functional dopants for organic photovoltaic devices.