Synthesis and Reactivity of an Alumanyl–Tin Species to Form an Al,N-Heteroallene Derivative

The molecular chemistry of metal-metal bonds is crucial for understanding the bonding and reactivity of metal-containing molecules as well as solid metals and their alloys, especially with respect to their application as catalysts for organic transformations and industrial processes. Despite the high efficiency of the recently developed nucleophilic alumanyl anions in the synthesis of diverse Al-metal bonds, the bonding between main group metals in a low oxidation state and the Al atom remains largely unexplored. This paper describes the reaction of an alumanyl anion with a chlorostannylene precursor to afford a compound with an unprecedented covalent Al-Sn bond. The lability of the covalent Al-Sn bond renders it reactive toward the insertion of carbodiimide, N<sub>2</sub>O, and phenylacetylene. Remarkably, the reaction with benzonitrile furnished an unprecedented Al,N-heteroallene species that contains a linear Al═N═C linkage.

Authors

Institutions

Publication Details

Journal
Journal of the American Chemical Society
Published
2024-10-08
DOI
https://doi.org/10.1021/jacs.4c11586
Citations
10
Primary Topic
Synthesis and characterization of novel inorganic/organometallic compounds
Type
article
Field-Weighted Citation Impact
1.58

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synthesis and Reactivity of an Alumanyl–Tin Species to Form an Al,N-Heteroallene Derivative

Makoto Yamashita, Genfeng Feng
10 citations
Journal of the American Chemical Society
Synthesis and characterization of novel inorganic/organometallic compounds
1.58
article

Synthesis and Reactivity of an Alumanyl–Tin Species to Form an Al,N-Heteroallene Derivative

Makoto Yamashita, Genfeng Feng
article en
10 citations

Abstract

The molecular chemistry of metal-metal bonds is crucial for understanding the bonding and reactivity of metal-containing molecules as well as solid metals and their alloys, especially with respect to their application as catalysts for organic transformations and industrial processes. Despite the high efficiency of the recently developed nucleophilic alumanyl anions in the synthesis of diverse Al-metal bonds, the bonding between main group metals in a low oxidation state and the Al atom remains largely unexplored. This paper describes the reaction of an alumanyl anion with a chlorostannylene precursor to afford a compound with an unprecedented covalent Al-Sn bond. The lability of the covalent Al-Sn bond renders it reactive toward the insertion of carbodiimide, N<sub>2</sub>O, and phenylacetylene. Remarkably, the reaction with benzonitrile furnished an unprecedented Al,N-heteroallene species that contains a linear Al═N═C linkage.

Journal of the American Chemical SocietyVol. 146(42)
Institute of Science Tokyo (JP), Nagoya University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 18%
Synthesis and characterization of novel inorganic/organometallic compounds
1.58
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Synthesis and Reactivity of an Alumanyl–Tin Species to Form an Al,N-Heteroallene Derivative — Makoto Yamashita, Genfeng Feng · Journal of the American Chemical Society (2024) | TGRS Research Map | TGRS