Solid-State NMR Spectroscopic Study of Coordination Compounds of XeF2with Metal Cations and the Crystal Structure of [Ba(XeF2)5][AsF6]2‖

2007 ◽  
Vol 46 (15) ◽  
pp. 6069-6077 ◽  
Author(s):  
Michael Gerken ◽  
Paul Hazendonk ◽  
Adriana Iuga ◽  
Jared Nieboer ◽  
Melita Tramšek ◽  
...  
ChemInform ◽  
2007 ◽  
Vol 38 (38) ◽  
Author(s):  
Michael Gerken ◽  
Paul Hazendonk ◽  
Adriana Iuga ◽  
Jared Nieboer ◽  
Melita Tramsek ◽  
...  

2019 ◽  
Vol 20 (15) ◽  
pp. 3656 ◽  
Author(s):  
Qian-Zhao Xu ◽  
Pavlo Bielytskyi ◽  
James Otis ◽  
Christina Lang ◽  
Jon Hughes ◽  
...  

Unlike canonical phytochromes, the GAF domain of cyanobacteriochromes (CBCRs) can bind bilins autonomously and is sufficient for functional photocycles. Despite the astonishing spectral diversity of CBCRs, the GAF1 domain of the three-GAF-domain photoreceptor all2699 from the cyanobacterium Nostoc 7120 is the only CBCR-GAF known that converts from a red-absorbing (Pr) dark state to a far-red-absorbing (Pfr) photoproduct, analogous to the more conservative phytochromes. Here we report a solid-state NMR spectroscopic study of all2699g1 in its Pr state. Conclusive NMR evidence unveils a particular stereochemical heterogeneity at the tetrahedral C31 atom, whereas the crystal structure shows exclusively the R-stereochemistry at this chiral center. Additional NMR experiments were performed on a construct comprising the GAF1 and GAF2 domains of all2699, showing a greater precision in the chromophore–protein interactions in the GAF1-2 construct. A 3D Pr structural model of the all2699g1-2 construct predicts a tongue-like region extending from the GAF2 domain (akin to canonical phytochromes) in the direction of the chromophore, shielding it from the solvent. In addition, this stabilizing element allows exclusively the R-stereochemistry for the chromophore-protein linkage. Site-directed mutagenesis performed on three conserved motifs in the hairpin-like tip confirms the interaction of the tongue region with the GAF1-bound chromophore.


2020 ◽  
Vol 124 (50) ◽  
pp. 27614-27620
Author(s):  
Marufa Zahan ◽  
He Sun ◽  
Sophia E. Hayes ◽  
Harald Krautscheid ◽  
Jürgen Haase ◽  
...  

2018 ◽  
Vol 73 (11) ◽  
pp. 793-801
Author(s):  
Aleksej Jochim ◽  
Christian Näther

AbstractReaction of Mn(NCS)2with pyrazole leads to the formation of three compounds with the compositions Mn(NCS)2(pyrazole)4(1), [Mn(NCS)2]2(pyrazole)6(2) and Mn(NCS)2(pyrazole)2(3). Compound1, already reported in the literature, consists of discrete complexes, in which the Mn(II) cations are octahedrally coordinated by four pyrazole ligands and two terminally N-bonded thiocyanate anions. In compound2each of the two Mn(II) cations are coordinated octahedrally by three pyrazole ligands and one terminal as well as two bridging thiocyanate anions, which link the metal cations into dimers. In compound3also octahedrally coordinated Mn(II) cations are present but they are linked into chainsviacentrosymmetric pairs ofμ-1,3-bridging thiocyanate anions. Upon heating compound1loses the pyrazole co-ligands stepwise and is transformed into the chain compound3viathe dimer2that is formed as an intermediate. Magnetic measurements on compounds2and3reveal dominating antiferromagnetic interactions, as already observed for 1D Mn(NCS)2coordination compounds with pyridine based co-ligands.


2017 ◽  
Vol 686 ◽  
pp. 7-11 ◽  
Author(s):  
Łukasz Szeleszczuk ◽  
Tomasz Gubica ◽  
Andrzej Zimniak ◽  
Dariusz M. Pisklak ◽  
Kinga Dąbrowska ◽  
...  

2016 ◽  
Vol 131 ◽  
pp. 364-372 ◽  
Author(s):  
Silke D. Gumbert ◽  
Meike Körbitzer ◽  
Edith Alig ◽  
Martin U. Schmidt ◽  
Michele R. Chierotti ◽  
...  

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