Tridentate Lewis-acids based on triphenylsilane

2017 ◽  
Vol 46 (5) ◽  
pp. 1645-1659 ◽  
Author(s):  
Janek Tomaschautzky ◽  
Beate Neumann ◽  
Hans-Georg Stammler ◽  
Andreas Mix ◽  
Norbert W. Mitzel

Triphenylsilanes are versatile propeller-shaped building blocks and have been used for the syntheses of several novel poly-Lewis-acids. The first solid-state structure of a bisma-silatriptycene as well as investigations in host–guest chemistry of a triple alane with a threefold amine are reported.

1993 ◽  
Vol 48 (10) ◽  
pp. 1381-1385 ◽  
Author(s):  
Kattesh V. Katti ◽  
Prahlad R. Singh ◽  
Charles L. Barnes ◽  
Kavita K. Katti ◽  
Karel Kopicka ◽  
...  

Reactions of the organometallic phosphinimine Ph3P=N-SiMe3 (1), with aqueous ReO4- and 188ReO4- yield the ion pairs Ph3P=NH2+MO4- (M=Re (2); 188Re (4)). The ion pairs undergo dehydration upon heating to produce the neutral Re(VII) species: Ph3P=N-MO3 (M=Re (3); 188Re (5)). The solid state structure of Ph3P=NH2+ReO4- (2) shows the presence of hydrogen bonding between the iminato hydrogen and the rhenium oxo center. The relevance of such reactions for the design of new radiopharmaceuticals is discussed


2008 ◽  
Vol 59 (11) ◽  
Author(s):  
Mircea Braban ◽  
Ionel Haiduc

The paper describes the solid state structure of a compound of composition [Cu(bipy)3][Cu(bipy)(ala) (ClO4)2]ClO4, in which both the cation and anion are octahedral complex species with copper(II) as coordination center. The cation contains three chelate rings formed by bipy; the anion contains in the quatorial plane a CuONC2 chelate ring formed by the alaninato ligand and a CuN2C2 chelate ring formed by bipy, with two monodentate perchorato ligands in axial positions completing the six-coordination. In the crystal p-p stackings lead to a supramolecular self-assembled structure.


2015 ◽  
Vol 19 (5) ◽  
pp. 469-474 ◽  
Author(s):  
Nicholas Bewick ◽  
Agata Arendt ◽  
Yan Li ◽  
S.awomir Szafert ◽  
Tadeusz Lis ◽  
...  

CrystEngComm ◽  
2021 ◽  
Author(s):  
Mainak Karmakar ◽  
Antonio Frontera ◽  
Shouvik Chattopadhyay

The formation of an infinite 1D assembly is governed by the H-bonding interactions in the solid state structure of the two zinc complexes. It has been analyzed energetically using DFT calculations and several computational tools.


Author(s):  
Senka Djaković ◽  
Silvija Maračić ◽  
Jasmina Lapić ◽  
Eduard Kovalski ◽  
Alexander Hildebrandt ◽  
...  

1990 ◽  
Vol 86 (4) ◽  
pp. 739 ◽  
Author(s):  
Giovanni Carturan ◽  
Stefano Enzo ◽  
Renzo Ganzerla ◽  
Maurizio Lenarda ◽  
Roberto Zanoni

1998 ◽  
Vol 53 (5-6) ◽  
pp. 625-627 ◽  
Author(s):  
Matthias Westerhausen ◽  
Wolfgang Schwarz

Abstract The reaction of potassium with hexamethyldi-stannane in a refluxing solvent mixture of toluene and tetrahydrofuran (ratio 10:1) yields the red tetrahydrofuran adduct of benzyl potassium (thf)[KCH2C6H5]2 due to the metalation of toluene by the potassium trimethylstannanide intermediate. The solid state structure of (thf)[KCH2C6H5]2 contains dimers with only one potassium coordinated to a tetrahydrofuran molecule. These dimers form a polymer through benzyl bridging with shortest K-C distances at 292 pm.


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