Back Cover: Synthesis, Structure, and Reactivity of Lewis Base Stabilized Plumbacyclopentadienylidenes (Chem. Eur. J. 50/2013). Issue 50 (9th December 2013)

• Record Type: Journal Article
• Authors: Saito, Masaichi; Akiba, Tomoki; Kaneko, Misumi; Kawamura, Toshiaki; Abe, Minori; Hada, Masahiko; Minoura, Mao
• Is Part Of: Chemistry. Volume 19:Issue 50(2013)
• Page Start: 17220
• Page End: 17220
• Publication Date: 2013-12-09
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201390201
• Languages: English
• ISSNs: 0947-6539

Abstract

<abstract abstract-type="graphical" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold>Plumbacyclopentadienylidenes </bold> in which the lead atom is coordinated to a variety of Lewis bases, including THF, exhibit interesting behavior and reactivity. In their Full Paper on <ext-link ext-link-type="doi" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">page 16946 ff.</ext-link>, M. Saito et al. show that the THF adduct, which is a rare example of a 10‐X‐4 species, reacts with trifluoroborane or trichlorogallane to afford fluoroborole and chlorogallole, respectively.<boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgg4t3t1sw6" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract>