TY  - JOUR
A1  - Sperlich, Eric
A1  - Köckerling, Martin
T1  - [Nb6Cl12(CH3OH)4(OCH3)2] ⋅ DABCO ⋅ 1.66 CH2Cl2
BT  - cluster units wrapped in a network of hydrogen bonds
JF  - Zeitschrift für anorganische und allgemeine Chemie : ZAAC = Journal of inorganic and general chemistry
N2  - An easy-to-do synthesis for the hexanuclear niobium cluster compound [Nb6Cl12(CH3OH)(4)(OCH3)(2)] . DABCO . 1.66 CH2Cl2 has been developed. An one-pot reaction between the cluster precursor [Nb6Cl14(H2O)(4)] . 4H(2)O and methanol with the addition of DABCO leads to the crystallization of the title compound in high yield within a few minutes. The single-crystal X-ray structure of this cluster compound has been determined. Very strong, nearly symmetric intercluster hydrogen bonds Nb-6-MeO...H...OMe-Nb-6 are present between the cluster units. A bridging co-crystalline DABCO molecule is also involved in a three-dimensional hydrogen-bonding network.
KW  - Niobium
KW  - Cluster
KW  - Hydrogen Bonds
KW  - Synthesis
KW  - Structure Determination
Y1  - 2021
U6  - https://doi.org/10.1002/zaac.202100138
SN  - 0044-2313
SN  - 1521-3749
VL  - 647
IS  - 18
SP  - 1759
EP  - 1763
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Shainyan, Bagrat A.
A1  - Tolstikova, Ljudmila L.
A1  - Schilde, Uwe
T1  - Simple methods for the preparation of N-triflyl guanidines and the structure of compounds with the CF3SO2N=C-N fragment
JF  - Journal of fluorine chemistry
N2  - Two novel and simple approaches to N-triflyl guanidines are elaborated. Owing to very strong conjugation the formally double C=N bond of TIN=C(NHR)(2) is longer than the formally single N-C bonds. Energetic effect of the triflylgroup on the conjugation in the N-C=N moiety is estimated to be >= 150 kcal/mol.
KW  - N-triflyl guanidines
KW  - Synthesis
KW  - Structure
KW  - X-ray
KW  - MP2 calculations
Y1  - 2012
U6  - https://doi.org/10.1016/j.fluchem.2011.12.004
SN  - 0022-1139
VL  - 135
IS  - 1
SP  - 261
EP  - 264
PB  - Elsevier
CY  - Lausanne
ER  - 
TY  - JOUR
A1  - Schwarze, Thomas
A1  - Traeger, Juliane
A1  - Kelling, Alexandra
A1  - Schilde, Uwe
A1  - Holdt, Hans-Jürgen
T1  - Macrocyclic dithiomaleonitriles for an efficient PdCl2 coordination
JF  - Inorganica chimica acta : the international inorganic chemistry journal
N2  - We have synthesized a set of new unsaturated macrocyclic dithioethers with an increasing number of flexible methylene units 1-7 (Scheme 2) to investigate the correlation between the ring size of these ligands, the chelation effect and the consequences for an efficient PdCl2 coordination. The dithioethers 1-7 and the complex [PdCl2(4)]center dot CHCl3 were characterized by X-ray diffraction analysis. The crystal structures of 1-7 show that 2-7 are better preorganized chelating ligands for an exocyclic PdCl2 coordination than 1. The chelation effect of 1-7, the orientation of the sulfur atoms and the S center dot center dot center dot S donor distances, are influenced by the flexibility of the methylene units. In this series the unsaturated macrocyclic ligands 5 and 6 are the best chelating ligands for an efficient PdCl2 coordination. Comparative solvent extraction experiments with mn-12S(2)O(2) (mn = maleonitrile) reveal that the low interface activity of the new ligands reduces the extraction rate. However, a comparison with open-chain dithiomaleonitriles shows the impact of the macrocyclic effect of 4 and 5 on the extraction yield.
KW  - Thioether ligands
KW  - Palladium
KW  - Synthesis
KW  - X-ray diffraction
KW  - Chelation effect
KW  - Extraction
Y1  - 2013
U6  - https://doi.org/10.1016/j.ica.2013.08.020
SN  - 0020-1693
SN  - 1873-3255
VL  - 408
IS  - 2
SP  - 53
EP  - 58
PB  - Elsevier
CY  - Lausanne
ER  -