Phosphacycles as Building Blocks for Main Group Cages

2013 ◽  
Vol 125 (12) ◽  
pp. 3565-3568 ◽  
Author(s):  
Nell S. Townsend ◽  
Sam R. Shadbolt ◽  
Michael Green ◽  
Christopher A. Russell
Keyword(s):  
1994 ◽  
Vol 49 (1) ◽  
pp. 43-49 ◽  
Author(s):  
Reinhard Hasselbring ◽  
Herbert W. Roesky ◽  
Andreas Heine ◽  
Dietmar Stalke ◽  
George M. Sheldrick

Abstract Acylic silylated phosphazenes of the type HN(PR2NSiMe3)2 (1) react quantitatively with molecules MMe3 (M = Al, Ga, In) under ring formation and CH4 evolution. The ring compounds N(PPh2NSiMe3)2AlMe2 (2 a) and N(PPh2NSiMe3)2InMe2 (4 a) have been investiga­ ted by X-ray structure determination. 2a and 4a crystallize in the space groups P 1̄ and P 31, respectively; they show different conformations regarding the cyclohexane framework. NMR spectroscopy of the nuclei in the chelating phosphazene ligand indicates decreasing Lewis acidity of the metal containing fragments in the series AlMe2 ≥ GaMe2 > InMe2.


2019 ◽  
Vol 48 (22) ◽  
pp. 7632-7643 ◽  
Author(s):  
Benjamin J. Frogley ◽  
Tobias L. Genet ◽  
Anthony F. Hill ◽  
Chee S. Onn

The reactions of [W(CBr)(CO)2(Tp*)] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate) with lithium alkynylselenolates LiSeCCR (R = SiMe3, SiiPr3, nBu, tBu, Ph, p-tolyl) afford the alkynylselenolatoalkylidyne complexes [W(CSeCCR)(CO)2(Tp*)].


CrystEngComm ◽  
2018 ◽  
Vol 20 (39) ◽  
pp. 5998-6004 ◽  
Author(s):  
Davin Tan ◽  
Zi Xuan Ng ◽  
Ying Sim ◽  
Rakesh Ganguly ◽  
Felipe García

Bench-top stable cis-cyclodiphosph(v/v)azanes are demonstrated to form robust R21(8) bifurcated hydrogen-bonds and PSe⋯Br halogen bonds. This work highlights the potential of cyclodiphosph(v/v)azane building blocks in creating new supramolecular assemblies.


2013 ◽  
Vol 52 (12) ◽  
pp. 3481-3484 ◽  
Author(s):  
Nell S. Townsend ◽  
Sam R. Shadbolt ◽  
Michael Green ◽  
Christopher A. Russell
Keyword(s):  

2021 ◽  
Author(s):  
Joel Häfliger ◽  
Keith Livingstone ◽  
Constantin Daniliuc ◽  
Ryan Gilmour

Simple α-(bromomethyl)styrenes can be processed to a variety of 1,1-difluorinated electrophilic building blocks via I(I)/I(III) catalysis. This inexpensive main group catalysis strategy employs p-TolI as an effective organocatalyst when combined...


2021 ◽  
Author(s):  
Weiyi Zhou ◽  
Nathan J. Yutronkie ◽  
Benoît H. Lessard ◽  
Jaclyn L. Brusso

Main-group phthalocyanines are an emerging class of organic semiconductors with versatile charge carriers in field-effect transistors. In this review, an overview is provided on the synthesis of these building blocks and device performances.


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