Coordination chemistry of stannylene-based Lewis pairs – insertion into M–Cl and M–C bonds. From base stabilized stannylenes to bidentate ligands

2018 ◽  
Vol 47 (1) ◽  
pp. 83-95 ◽  
Author(s):  
K. M. Krebs ◽  
S. Freitag ◽  
J.-J. Maudrich ◽  
H. Schubert ◽  
P. Sirsch ◽  
...  

The coordination chemistry of intramolecular stannylene phosphorus Lewis pairs incorporated into four or three membered ring molecules is presented.

Author(s):  
Pedro Guerra Demingos ◽  
Naira Maria Balzaretti ◽  
André Muniz

Carbon nanothreads are one-dimensional materials obtained by controlled compression of aromatic molecules. Benzene and other six-membered ring molecules are normally used as precursors, but recent experiments have shown that carbon...


Molecules ◽  
2020 ◽  
Vol 25 (24) ◽  
pp. 5950
Author(s):  
Steffen B. Mogensen ◽  
Mercedes K. Taylor ◽  
Ji-Woong Lee

Pyrazole, a member of the structural class of azoles, exhibits molecular properties of interest in pharmaceuticals and materials chemistry, owing to the two adjacent nitrogen atoms in the five-membered ring system. The weakly basic nitrogen atoms of deprotonated pyrazoles have been applied in coordination chemistry, particularly to access coordination polymers and metal-organic frameworks, and homocoupling reactions can in principle provide facile access to bipyrazole ligands. In this context, we summarize recent advances in homocoupling reactions of pyrazoles and other types of azoles (imidazoles, triazoles and tetrazoles) to highlight the utility of homocoupling reactions in synthesizing symmetric bi-heteroaryl systems compared with traditional synthesis. Metal-free reactions and transition-metal catalyzed homocoupling reactions are discussed with reaction mechanisms in detail.


1972 ◽  
Vol 42 (1) ◽  
pp. 112-126 ◽  
Author(s):  
F. Baltagi ◽  
A. Bauder ◽  
T. Ueda ◽  
Hs.H. Günthard
Keyword(s):  

2001 ◽  
Vol 56 (8) ◽  
pp. 711-718 ◽  
Author(s):  
Stefan D. Nogai ◽  
Annette Schier ◽  
Hubert Schmidbaur

The four ternary gallium(III) chalcogenide halides GaEX with E = S, Se and X = Cl, Br can be prepared a) from the binary gallium(III) chalcogenides Ga2E3 and halides Ga2X6, b) from gallium(I) tetrahalogallates(III) GafGaX4] and the chalcogen E, and c) from gallium metal and the dichalcogen dihalides E2X2. The new method c) was shown to be the most convenient preparation. The products are readily soluble in pyridine to give trinuclear molecular complexes [GaEX·Py]3 which are not volatile without decomposition, but can be purified by crystallization. The structures have been determined by single crystal X-ray diffraction techniques. The two chlorides are isostructural and show twisted tub-form six-membered ring molecules with the pyridine donors in axial positions. The two bromides are also isostructural, but with the pyridine ligands in two axial and one equatorial positions


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