Evidence map›Paper›PMID 27336303›Full record

ArticlePloS one2016

Aminoxyl Radicals of B/P Frustrated Lewis Pairs: Refinement of the Spin-Hamiltonian Parameters by Field- and Temperature-Dependent Pulsed EPR Spectroscopy.

Marcos de Oliveira, Robert Knitsch, Muhammad Sajid, Annika Stute, Lisa-Maria Elmer, Gerald Kehr, Gerhard Erker, Claudio J Magon, Gunnar Jeschke, Hellmut Eckert

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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.

Marcos de OliveiraInstituto de Física de São Carlos, Universidade de São Paulo, P.O. Box 369, 13560-970, São Carlos, São Paulo, Brazil.
Robert KnitschInstitut für Physikalische Chemie, WWU Münster, Corrensstr. 30, D 48149 Münster, Germany.
Muhammad SajidOrganisch-Chemisches Institut, WWU Münster, Corrensstr. 40, D 48149 Münster, Germany.
Annika StuteOrganisch-Chemisches Institut, WWU Münster, Corrensstr. 40, D 48149 Münster, Germany.
Lisa-Maria ElmerOrganisch-Chemisches Institut, WWU Münster, Corrensstr. 40, D 48149 Münster, Germany.
Gerald KehrOrganisch-Chemisches Institut, WWU Münster, Corrensstr. 40, D 48149 Münster, Germany.
Gerhard ErkerOrganisch-Chemisches Institut, WWU Münster, Corrensstr. 40, D 48149 Münster, Germany.
Claudio J MagonInstituto de Física de São Carlos, Universidade de São Paulo, P.O. Box 369, 13560-970, São Carlos, São Paulo, Brazil.
Gunnar JeschkeLaboratorium für Physikalische Chemie, ETH Zürich, Vladimir-Prelog-Weg 2, 8049 Zürich, Switzerland.
Hellmut EckertInstituto de Física de São Carlos, Universidade de São Paulo, P.O. Box 369, 13560-970, São Carlos, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Q-band and X-band pulsed electron paramagnetic resonance spectroscopic methods (EPR) in the solid state were employed to refine the parameters characterizing the anisotropic interactions present in six nitroxide radicals prepared by N,N addition of NO to various borane-phosphane frustrated Lewis pairs (FLPs). The EPR spectra are characterized by the g-anisotropy as well as by nuclear hyperfine coupling between the unpaired electron and the 11B/10B, 14N and 31P nuclear magnetic moments. It was previously shown that continuous-wave spectra measured at X-band frequency (9.5 GHz) are dominated by the magnetic hyperfine coupling to 14N and 31P, whereas the g-tensor values and the 11B hyperfine coupling parameters cannot be refined with high precision from lineshape fitting. On the other hand, the X-band electron spin echo envelope modulation (ESEEM) and hyperfine sublevel correlation (HYSCORE) spectra are completely dominated by the nuclear hyperfine coupling to the 11B nuclei, allowing a selective determination of their interaction parameters. In the present work this analysis has been further validated by temperature dependent ESEEM measurements. In addition, pulsed EPR data measured in the Q-band (34 GHz) are reported, which present an entirely different situation: the g-tensor components can be measured with much higher precision, and the ESEEM and HYSCORE spectra contain information about all of the 10B, 11B, 14N and 31P hyperfine interaction parameters. Based on these new results, we report here high-accuracy and precision data of the EPR spin Hamiltonian parameters measured on six FLP-NO radical species embedded in their corresponding hydroxylamine host structures. While the ESEEM spectra at Q-band frequency turn out to be very complex (due to the multinuclear contribution to the overall signal) in the HYSCORE experiment the extension over two dimensions renders a better discrimination between the different nuclear species, and the signals arising from hyperfine coupling to 10B, 11B, 14N and 31P nuclei can be individually analyzed.

Indexed as

Electron Spin Resonance SpectroscopyModels, TheoreticalAlgorithmsTemperature

Identifiers

PMID27336303
PMCPMC4918942

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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.