Themed collection Frontiers in Main Group Chemistry

2 items
Open Access Research Article

Accessing phosphonioacetylide chemistry: isolable alkali metal precursors for rod-shaped carbon donor complexes

The high reactivity of a sterically accessible phosphonioacetylide was tamed via alkali metal coordination. The resulting complexes are precursors for introducing the rod-shaped, strongly electron-donating ligand into transition metal complexes.

Graphical abstract: Accessing phosphonioacetylide chemistry: isolable alkali metal precursors for rod-shaped carbon donor complexes
Open Access Research Article

Silagermylenation of C[double bond, length as m-dash]O bonds and radical fragmentation of CO2-expanded bis(germylene) by a cyclic (alkyl)(amino)carbene

CO2 and EtNCO are inserted into the Ge–Si bonds of an NHC-bis(germylene) with nucleophilic Ge(II) lone-pairs and an electrophilic para-silylenearylene backbone. CAAC-induced fragmentation yields a germylene with a tethered CAAC-radical.

Graphical abstract: Silagermylenation of C [[double bond, length as m-dash]] O bonds and radical fragmentation of CO2-expanded bis(germylene) by a cyclic (alkyl)(amino)carbene
From the themed collection: Frontiers in Main Group Chemistry
2 items

About this collection

Welcome to Inorganic Chemistry Frontiers themed collection on Frontiers in Main Group Chemistry.

Main group elements are among the most abundant and essential constituents of the universe, integral to a myriad of applications that span from supporting life to driving innovative technological advancements. This collection aims to showcase cutting-edge research that illustrates novel functionalities and reactivities of main-group compounds, contributing significantly to both fundamental science and practical applications.

Guest Editors: Douglas W. Stephan (University of Toronto), Viktoria H. Gessner (Ruhr-University Bochum) and Liu Leo Liu (Southern University of Science and Technology)

More articles will be added as soon as they are published.


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