Hydrodechlorination of Dichloromethane by a Metal‐Free Triazole‐Porphyrin Electrocatalyst: Demonstration of Main‐Group Element Electrocatalysis

2021 ◽  
Author(s):  
Caroline Williams ◽  
Amir Lashgari ◽  
Nilakshi Devi ◽  
Marcus Ang ◽  
Ashwin Chaturvedi ◽  
...  
Keyword(s):  
Main Group ◽  
Group Element ◽  
Metal Free ◽  
Main Group Element

Hydrodechlorination of Dichloromethane by a Metal-Free Triazole-Porphyrin Electrocatalyst: Demonstration of Main-Group Element Electrocatalysis

2020 ◽  
Author(s):  
Caroline Williams ◽  
Amir Lashgari ◽  
Marcus Ang ◽  
Pranita Dhungana ◽  
Jianbing Jiang
Keyword(s):  
Current Density ◽  
Catalytic Reaction ◽  
Reaction Mechanisms ◽  
Main Group ◽  
Group Element ◽  
Electrocatalytic Reduction ◽  
Faradaic Efficiency ◽  
Metal Free ◽  
Main Group Element ◽  
Proton Source

<p>In this work, the electrocatalytic reduction of dichloromethane (CH<sub>2</sub>Cl<sub>2</sub>) into hydrocarbons involving a main group element-based molecular triazole-porphyrin electrocatalyst H2PorT8 is reported. This catalyst converted CH<sub>2</sub>Cl<sub>2</sub> in acetonitrile to various hydrocarbons (methane, ethane, and ethylene) with a Faradaic efficiency of 70% and current density of –13 mA/cm<sup>2</sup> at a potential of –2.2 V vs. Fc/Fc<sup>+</sup> using water as a proton source. The findings of this study and its mechanistic interpretations demonstrated that H2PorT8 was an efficient and stable catalyst for the hydrodechlorination of CH<sub>2</sub>Cl<sub>2</sub> and that main group catalysts could be potentially used for exploring new catalytic reaction mechanisms.</p>

Hydrodechlorination of Dichloromethane by a Metal-Free Triazole-Porphyrin Electrocatalyst: Demonstration of Main-Group Element Electrocatalysis

2020 ◽  
Author(s):  
Caroline Williams ◽  
Amir Lashgari ◽  
Marcus Ang ◽  
Pranita Dhungana ◽  
Jianbing Jiang
Keyword(s):  
Current Density ◽  
Catalytic Reaction ◽  
Reaction Mechanisms ◽  
Main Group ◽  
Group Element ◽  
Electrocatalytic Reduction ◽  
Faradaic Efficiency ◽  
Metal Free ◽  
Main Group Element ◽  
Proton Source

<p>In this work, the electrocatalytic reduction of dichloromethane (CH<sub>2</sub>Cl<sub>2</sub>) into hydrocarbons involving a main group element-based molecular triazole-porphyrin electrocatalyst H2PorT8 is reported. This catalyst converted CH<sub>2</sub>Cl<sub>2</sub> in acetonitrile to various hydrocarbons (methane, ethane, and ethylene) with a Faradaic efficiency of 70% and current density of –13 mA/cm<sup>2</sup> at a potential of –2.2 V vs. Fc/Fc<sup>+</sup> using water as a proton source. The findings of this study and its mechanistic interpretations demonstrated that H2PorT8 was an efficient and stable catalyst for the hydrodechlorination of CH<sub>2</sub>Cl<sub>2</sub> and that main group catalysts could be potentially used for exploring new catalytic reaction mechanisms.</p>

Catalytic Fluorination of Boron Compounds at a Bismuth Redox Platform

2019 ◽  
Author(s):  
Oriol Planas ◽  
Feng Wang ◽  
Markus Leutzsch ◽  
Josep Cornella
Keyword(s):  
Transition Metal ◽  
Main Group ◽  
Group Element ◽  
Oxidation States ◽  
Boron Compounds ◽  
Main Text ◽  
Main Group Element ◽  
Rational Ligand Design ◽  
Supplementary Material

The ability of bismuth to maneuver between different oxidation states in a catalytic redox cycle, mimicking the canonical organometallic steps associated to a transition metal, is an elusive and unprecedented approach in the field of homogeneous catalysis. Herein we present a catalytic protocol based on bismuth, a benign and sustainable main-group element, capable of performing every organometallic step in the context of oxidative fluorination of boron compounds; a territory reserved to transition metals. A rational ligand design featuring hypervalent coordination together with a mechanistic understanding of the fundamental steps, permitted a catalytic fluorination protocol based on a Bi(III)/Bi(V) redox couple, which represents a unique example where a main-group element is capable of outperforming its transition metal counterparts.<br>A main text and supplementary material have been attached as pdf files containing all the methodology, techniques and characterization of the compounds reported.<br>

scholarly journals On the Coordination Role of Pyridyl-Nitrogen in the Structural Chemistry of Pyridyl-Substituted Dithiocarbamate Ligands

Crystals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 286
Author(s):  
Edward R.T. Tiekink
Keyword(s):  
Transition Metal ◽  
Main Group ◽  
Group Element ◽  
Systematic Research ◽  
Pyridyl Nitrogen ◽  
General Observation ◽  
Supramolecular Architectures ◽  
Main Group Element ◽  
Metal Dithiocarbamates

A search of the Cambridge Structural Database was conducted for pyridyl-substituted dithiocarbamate ligands. This entailed molecules containing both an NCS2− residue and pyridyl group(s), in order to study their complexation behavior in their transition metal and main group element crystals, i.e., d- and p-block elements. In all, 73 different structures were identified with 30 distinct dithiocarbamate ligands. As a general observation, the structures of the transition metal dithiocarbamates resembled those of their non-pyridyl derivatives, there being no role for the pyridyl-nitrogen atom in coordination. While the same is true for many main group element dithiocarbamates, a far greater role for coordination of the pyridyl-nitrogen atoms was evident, in particular, for the heavier elements. The participation of pyridyl-nitrogen in coordination often leads to the formation of dimeric aggregates but also one-dimensional chains and two-dimensional arrays. Capricious behaviour in closely related species that adopted very different architectures is noted. Sometimes different molecules comprising the asymmetric-unit of a crystal behave differently. The foregoing suggests this to be an area in early development and is a fertile avenue for systematic research for probing further crystallization outcomes and for the rational generation of supramolecular architectures.

scholarly journals Antimony Complexes for Electrocatalysis: Activity of a Main-Group Element in Proton Reduction

2017 ◽  
Vol 56 (31) ◽  
pp. 9111-9115 ◽  
Author(s):  
Jianbing Jiang ◽  
Kelly L. Materna ◽  
Svante Hedström ◽  
Ke R. Yang ◽  
Robert H. Crabtree ◽  
...  
Keyword(s):  
Main Group ◽  
Group Element ◽  
Proton Reduction ◽  
Main Group Element ◽  
Antimony Complexes

Theoretical Investigation of Main-Group Element Hydride Insertion into Phosphorus-Heterocyclic Carbenes (PHCs)

2020 ◽  
Vol 73 (8) ◽  
pp. 787
Author(s):  
Khalidah H. M. Al Furaiji ◽  
Andrew Molino ◽  
Jason L. Dutton ◽  
David J. D. Wilson
Keyword(s):  
Computational Study ◽  
Ring Expansion ◽  
Heterocyclic Ring ◽  
Main Group ◽  
Heterocyclic Carbenes ◽  
Group Element ◽  
Steric Effects ◽  
Main Group Element ◽  
Theoretical Investigations ◽  
Electronic And Steric Effects

Initial reports of ring expansion reactions (RER) of N-heterocyclic carbenes (NHCs) with main-group element hydrides have led to several synthetic and theoretical investigations, which include reports of insertion by Be, B, Al, Si, and Zn hydrides. The RERs generally lead to insertion of the heteroatom into the endocyclic C–N bond with formation of an expanded heterocyclic ring. Following the recent isolation of a P-heterocyclic carbene (PHC), here we report results from a computational study (RI-SCS-MP2/def2-TZVP//M06–2X/def2-TZVP) of RERs with a series of PHCs for the ring-insertion of silicon (SiH4, SiH2Ph2) and boron (BH3, BH2NMe2) hydrides. In order to explore the roles of both electronic and steric effects on PHCs and their reactivity, a series of P-substituent PHCR (R=H, Me, Ph, and bulky Ar groups) were investigated. Bulky R groups serve to maximise ring planarity and the σ-donating capability of the PHC. For RER, the PHC analogues exhibit facile initial hydride transfer from the main-group hydrides to the carbene carbon, with barriers that are substantially lower than with NHCs. However, the full ring insertion mechanisms for PHCs are, in general, kinetically unfavourable due to a large barrier associated with the ring-expansion step. While bulky P-substituents maximise heterocycle planarity towards that of NHCs, the RER reactivity with bulky PHCs does not reflect that of an NHC.

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