Evidence map›Paper›PMID 37886624›Full record

ArticleOrganometallics2023

Iron(II)-Catalyzed Activation of Si-N and Si-O Bonds Using Hydroboranes.

Mirela A Farcaş-Johnson, Danila Gasperini, Andrew K King, Sakshi Mohan, Adam N Barrett, Samantha Lau, Mary F Mahon, Yann Sarazin, Sara H Kyne, Ruth L Webster

Open access · hybridAbstract read
In one paragraph

Article in Organometallics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Mirela A Farcaş-JohnsonDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Danila GasperiniDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Andrew K KingDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Sakshi MohanInstitut des Sciences Chimiques de Rennes, Université de Rennes, Campus de Beaulieu, 35042 Rennes, France.
Adam N BarrettDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Samantha LauDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.ORCID https://orcid.org/0000-0001-9936-117X
Mary F MahonDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Yann SarazinInstitut des Sciences Chimiques de Rennes, Université de Rennes, Campus de Beaulieu, 35042 Rennes, France.
Sara H KyneSchool of Chemistry, Faculty of Science, University of New South Wales, Sydney, NSW 2052, Australia.ORCID https://orcid.org/0000-0002-6995-9311
Ruth L WebsterDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.ORCID https://orcid.org/0000-0001-9199-7579
University of Bath · GBInstitut des Sciences Chimiques de Rennes · FRUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the activation and functionalization of Si-N bonds with pinacol borane catalyzed by a three-coordinate iron(II) β-diketiminate complex. The reactions proceed via the mild activation of silazanes to yield useful hydrosilanes and aminoboranes. The reaction is studied by kinetic analysis, along with a detailed investigation of decomposition pathways using catecholborane as an analogue of the pinacol borane used in catalysis. We have extended the methodology to develop a polycarbosilazane depolymerization strategy, which generates hydrosilane quantitatively along with complete conversion to the Bpin-protected diamine. The analogous Si-O bond cleavage can also be achieved with heating, using silyl ether starting materials to generate hydrosilane and alkoxyborane products. Depolymerization of poly(silyl ether)s using our strategy successfully converts the polymer to 90% Bpin-protected alcohols.

Identifiers

PMID37886624
PMCPMC10598884
OpenAlexW4387342723

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.