Back Cover: Synthesis, Structure, and Reactivity of Lewis Base Stabilized Plumbacyclopentadienylidenes (Chem. Eur. J. 50/2013) | Zendy

Saito Masaichi | Zendy; Akiba Tomoki | Zendy; Kaneko Misumi | Zendy; Kawamura Toshiaki | Zendy; Abe Minori | Zendy; Hada Masahiko | Zendy; Minoura Mao | Zendy

Premium

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

Author(s) -

Saito Masaichi,

Akiba Tomoki,

Kaneko Misumi,

Kawamura Toshiaki,

Abe Minori,

Hada Masahiko,

Minoura Mao

Publication year - 2013

Publication title -

chemistry – a european journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.687

H-Index - 242

eISSN - 1521-3765

pISSN - 0947-6539

DOI - 10.1002/chem.201390201

Subject(s) - adduct , lewis acids and bases , reactivity (psychology) , frustrated lewis pair , cover (algebra) , chemistry , atom (system on chip) , polymer chemistry , organic chemistry , catalysis , computer science , medicine , mechanical engineering , alternative medicine , pathology , engineering , embedded system

Plumbacyclopentadienylidenes 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 page 16946 ff. , 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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research