TY  - JOUR
A1  - Sperlich, Eric
A1  - Köckerling, Martin
T1  - [Nb6Cl14(pyrazine)(4)], a versatile precursor for ligand-supported hexanuclear niobium cluster compounds: synthesis, characterization, follow-up reactions, and intermolecular interactions
JF  - Inorganic chemistry
N2  - The compound [Nb6Cl14(pyrazine)(4)]center dot 2CH(2)Cl(2) (1) was investigated for its suitability as a starting compound for new ligand-supported hexanuclear niobium cluster compounds. The synthesis, stability to air and increased temperature, solubility and usability for subsequent reactions of 1, and purification and separation of the reaction products are discussed. The compounds with cluster units [Nb6Cl14L4], where L = iso-quinoline N-oxides (2), 1,1-dimethylethylenediamines (3), or thiazoles (4), and [Nb6Cl14(PEt3)(3.76)(Et3PO)(0.24)]-[Nb6Cl14(MeCN)(4)]center dot 4MeCN (5) are presented as follow-up products. The crystal structures of compounds 1-5 are analyzed, and the structures are discussed with respect to their intraand intermolecular bonding situations and crystal packing. In addition to hydrogen bonds and pi-pi interactions, the appearance of chalcogen and halogen bonds and lone pair-pi interactions between Nb-6 cluster units was observed for the first time.
KW  - Cluster chemistry
KW  - crystals
KW  - ligands
KW  - molecules
KW  - transition metals
Y1  - 2022
U6  - https://doi.org/10.1021/acs.inorgchem.1c03109
SN  - 0020-1669
SN  - 1520-510X
VL  - 61
IS  - 5
SP  - 2409
EP  - 2420
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Arya, Pooja
A1  - Jelken, Joachim
A1  - Lomadze, Nino
A1  - Santer, Svetlana
A1  - Bekir, Marek
T1  - Kinetics of photo-isomerization of azobenzene containing surfactants
JF  - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistry
N2  - We report on photoisomerization kinetics of azobenzene containing surfactants in aqueous solution. The surfactant molecule consists of a positively charged trimethylammonium bromide head group, a hydrophobic spacer connecting via 6 to 10 CH2 groups to the azobenzene unit, and the hydrophobic tail of 1 and 3CH(2) groups. Under exposure to light, the azobenzene photoisomerizes from more stable trans- to metastable cis-state, which can be switched back either thermally in dark or by illumination with light of a longer wavelength. The surfactant isomerization is described by a kinetic model of a pseudo first order reaction approaching equilibrium, where the intensity controls the rate of isomerization until the equilibrated state. The rate constants of the trans-cis and cis-trans photoisomerization are calculated as a function of several parameters such as wavelength and intensity of light, the surfactant concentration, and the length of the hydrophobic tail. The thermal relaxation rate from cis- to trans-state is studied as well. The surfactant isomerization shows a different kinetic below and above the critical micellar concentration of the trans isomer due to steric hindrance within the densely packed micelle but does not depend on the spacer length.
KW  - genomic DNA conformation
KW  - water-interface
KW  - light photocontrol
KW  - driven
KW  - manipulation
KW  - photoisomerization
KW  - molecules
Y1  - 2020
U6  - https://doi.org/10.1063/1.5135913
SN  - 0021-9606
SN  - 1089-7690
VL  - 152
IS  - 2
PB  - American Institute of Physics
CY  - Melville
ER  -