ArticleAngewandte Chemie (International ed. in English)2019
Superelectrophilicity of 1,2-Azaborine: Formation of Xenon and Carbon Monoxide Adducts.
Article in Angewandte Chemie (International ed. in English), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- Understanding the Electronic Structure and Diels-Alder Reactivity of Nitrilium-TypeThe Journal of organic chemistry · 2026Article
- A Nitrilium-TypeJournal of the American Chemical Society · 2025Article
- Strain induced reactivity of cyclic iminoboranes: the (2 + 2) cycloaddition of a 1Chemical science · 2024Article
- Solution Phase Reactivity of Dibenzo[c,e][1,2]azaborinine: Activation and Insertion into Si-E Single Bonds (E=H, OSi(CHChemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- Superelectrophiles: Recent Advances.Molecules (Basel, Switzerland) · 2020Review
- Noble-Gas Chemistry More than Half a Century after the First Report of the Noble-Gas Compound.Molecules (Basel, Switzerland) · 2020Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
The BN analogue of ortho-benzyne, 1,2-azaborine, is shown to bind carbon monoxide and a xenon atom under matrix isolation conditions, demonstrating its strongly Lewis acidic superelectrophilic nature. The Lewis acid-base complexes involving CO and Xe can be cleaved photochemically and reformed by mildly annealing the matrices. The interaction energy of 1,2-azaborine with Xe is 3 kcal mol
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Registered trials
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