Recent advances in the chemistry of the Group 13 metals: hydride derivatives and compounds involving multiply bonded Group 13 metal atoms

1999 ◽  
Vol 189 (1) ◽  
pp. 59-100 ◽  
Author(s):  
A Downs
2002 ◽  
Vol 6 (15) ◽  
pp. 1469-1494 ◽  
Author(s):  
Toshihiro Murafuji ◽  
Kei Kurotobi ◽  
Norihiro Nakamura ◽  
Yoshikazu Sugihara

Synthesis ◽  
2017 ◽  
Vol 49 (16) ◽  
pp. 3511-3534 ◽  
Author(s):  
Tsuyoshi Taniguchi

Heteroatom-centered radicals show versatile reactivity and offer useful synthetic methods in organic chemistry. The development of new approaches for forming heteroatom-centered radicals has recently expanded the practicality of radical chemistry for synthesis. This review focuses on recent advances in reactions of representative heteroatom-centered radicals.1 Introduction2 Group 17 Elements: Chlorine and Bromine Radicals3 Group 15 and Group 16 Elements3.1 Nitrogen- and Oxygen-Centered Radicals3.2 Phosphorus- and Sulfur-Centered Radicals3.3 Other Radicals4 Group 14 Elements: Silicon-Centered Radicals5 Group 13 Elements: Boron-Centered Radicals6 Conclusion


2015 ◽  
Vol 2015 ◽  
pp. 1-23 ◽  
Author(s):  
Xiaochao Qu ◽  
Yichen Li ◽  
Lei Li ◽  
Yanran Wang ◽  
Jingning Liang ◽  
...  

Fluorescent gold nanoclusters (AuNCs) have been extensively studied due to their unique construction and distinctive properties, which place them between single metal atoms and larger nanoparticles. The dimension of AuNCs is comparable to the Fermi wavelength of electrons, which lead to size-dependent fluorescence and other molecule-like properties. In this review, we summarize various synthesis strategies of fluorescent AuNCs and recent advances of biological applications such as biosensing, biolabeling, and bioimaging. The synthetic methods are considered as two routes: “Atoms to Clusters” and “Nanoparticles to Clusters.” The surface functionalization of AuNCs is described as the precondition for making future bioapplications possible, which can eventually influence their stability, biocompatibility, and other properties. And then we focus on the recent advances of AuNCs-based applications in biological sensing, biolabeling, and bioimaging and finally discuss the current challenges of AuNCs in controllable synthesis and biological application.


1998 ◽  
Vol 76 (4) ◽  
pp. 400-406 ◽  
Author(s):  
Helen A Joly ◽  
Maria Kepes ◽  
Natalie Roy ◽  
Jason Prpic

Group 13 metal atoms were reacted with aromatic alkenes in a specialized metal atom reactor known as a "rotating cryostat." The nature of the intermediates formed was deduced from a GC-MS study of their hydrolysis and deuterolysis products. The product studies suggest that 2-phenylaluminacyclopropane, cis- and trans-3,4-diphenylaluminacyclopentane, and cis- and trans- 2,4-diphenylaluminacyclopentane are formed when Al atoms react with styrene, and 2-methyl-2-phenylaluminacyclopropane and 3,4-dimethyl- 3,4-diphenylaluminacyclopentane are formed when Al atoms react with α -methylstyrene. These findings are consistent with the radicals detected in the EPR spectroscopic studies of Al-alkene reaction mixtures prepared under similar conditions. Mechanisms for the formation of the organoaluminium intermediates are discussed. Analogous organogallium intermediates are formed when gallium atoms react with styrene. The reductive coupling of styrene did not occur when In and Tl atoms were used. Only trace quantities of phenylethane were detected in the hydrolyzed reaction mixture.Key words: Group 13 metal atoms, aluminium atoms, organoaluminium intermediates, metal atom reactions.


2004 ◽  
Vol 108 (24) ◽  
pp. 5169-5174 ◽  
Author(s):  
Xuefeng Wang ◽  
Bret Wolfe ◽  
Lester Andrews

Polyhedron ◽  
2002 ◽  
Vol 21 (5-6) ◽  
pp. 473-488 ◽  
Author(s):  
Anthony J Downs ◽  
Hans-Jörg Himmel ◽  
Laurent Manceron

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