Evidence map›Paper›PMID 27598037›Full record

ArticleJournal of the American Chemical Society2016

The Mechanism of N-N Double Bond Cleavage by an Iron(II) Hydride Complex.

Sarina M Bellows, Nicholas A Arnet, Prabhuodeyara M Gurubasavaraj, William W Brennessel, Eckhard Bill, Thomas R Cundari, Patrick L Holland

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Facile N═N Bond Cleavage of Cis-Azobenzene with Bis-silylenes.Angewandte Chemie (International ed. in English) · 2025
    Article
  3. Article
  4. Article
  5. Terminal Hydride Complex of High-Spin Mn.Journal of the American Chemical Society · 2024
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  13. An S =Journal of the American Chemical Society · 2018
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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

7 authors at 4 institutions in 2 countries.

Sarina M BellowsDepartment of Chemistry, University of Rochester , Rochester, New York 14627, United States.
Nicholas A ArnetDepartment of Chemistry, Yale University , New Haven, Connecticut 06520, United States.
Prabhuodeyara M GurubasavarajDepartment of Chemistry, University of Rochester , Rochester, New York 14627, United States.
William W BrennesselDepartment of Chemistry, University of Rochester , Rochester, New York 14627, United States.
Eckhard BillMax Planck Institute for Chemical Energy Conversion , Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany.
Thomas R CundariDepartment of Chemistry and CASCaM, University of North Texas , Denton, Texas 76203, United States.
Patrick L HollandDepartment of Chemistry, University of Rochester , Rochester, New York 14627, United States.
University of Rochester · USMax Planck Institute for Chemical Energy Conversion · DEUniversity of North Texas · USYale University · US

Funding

Low-Coordinate Synthetic Models for Nitrogenase ActivityR01GM065313 · NIGMS · YALE UNIVERSITY · PI PATRICK L HOLLAND · 2004 to 2026
$6.4M
NIGMS NIH HHS R01 GM065313
6 · The paper itself

Abstract

The use of hydride species for substrate reductions avoids strong reductants, and may enable nitrogenase to reduce multiple bonds without unreasonably low redox potentials. In this work, we explore the N═N bond cleaving ability of a high-spin iron(II) hydride dimer with concomitant release of H2. Specifically, this diiron(II) complex reacts with azobenzene (PhN═NPh) to perform a four-electron reduction, where two electrons come from H2 reductive elimination and the other two come from iron oxidation. The rate law of the H2 releasing reaction indicates that diazene binding occurs prior to H2 elimination, and the negative entropy of activation and inverse kinetic isotope effect indicate that H-H bond formation is the rate-limiting step. Thus, substrate binding causes reductive elimination of H2 that formally reduces the metals, and the metals use the additional two electrons to cleave the N-N multiple bond.

Indexed as

Azo CompoundsCatalysisFerrous CompoundsModels, MolecularMolecular StructureNitrogenazobenzeneAzo CompoundsFerrous CompoundsNitrogen

Identifiers

PMID27598037
PMCPMC5499983
OpenAlexW2507318159

What OpenQuestion holds

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LicenceTDM
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.