O–H and (CO)N–H bond weakening by coordination to Fe(ii)-Reference-Cited by-同舟云学术

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O–H and (CO)N–H bond weakening by coordination to Fe(ii)

Published:2019 Issue:6 Volume:48 Page:2179-2189
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Resa Sandra¹²³⁴,Millán Alba¹²³⁴^ORCID,Fuentes Noelia⁵⁶⁷⁴^ORCID,Crovetto Luis⁸⁹¹⁰³⁴^ORCID,Luisa Marcos M.¹¹⁶⁷⁴^ORCID,Lezama Luis¹²¹³¹⁴¹⁵¹⁶^ORCID,Choquesillo-Lazarte Duane¹⁷¹⁸¹⁹⁴^ORCID,Blanco Victor¹²³⁴^ORCID,Campaña Araceli G.¹²³⁴^ORCID,Cárdenas Diego J.⁵⁶⁷⁴^ORCID,Cuerva Juan M.¹²³⁴^ORCID

Affiliation:

1. Departamento Química Orgánica

2. Universidad de Granada (UGR)

3. 18071 Granada

4. Spain

5. Departamento de Química Orgánica

6. Universidad Autónoma de Madrid. Ciudad Universitaria de Cantoblanco

7. 28049 Madrid

8. Departamento de Fisicoquímica

9. Facultad de Farmacia

10. (UGR)

11. Departamento de Química

12. Departamento de Química Inorgánica

13. Facultad de Ciencia y Tecnología

14. Universidad del País Vasco

15. UPV/EHU

16. 48940 Leioa

17. Laboratorio de Estudios Cristalográficos

18. Instituto Andaluz de Ciencias de la Tierra (CSIC-UGR)

19. 18100 Armilla

Abstract

Coordination of hydroxyl/amide groups to Fe(ii) diminishes BDFEs of O–H and (CO)N–H bonds down to 76.0 and 80.5 kcal mol⁻¹ respectively.

Funder

Ministerio de Economía y Competitividad

Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía

Ministerio de Economía, Industria y Competitividad, Gobierno de España

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/DT/C8DT04689A

Reference80 articles.

1. Thermochemistry of Proton-Coupled Electron Transfer Reagents and its Implications

2. Copper–Oxygen Complexes Revisited: Structures, Spectroscopy, and Reactivity

3. The reactivity of the active metal oxo and hydroxo intermediates and their implications in oxidations

4. Mechanism of Rapid Electron Transfer during Oxygen Activation in the R2 Subunit of Escherichia coli Ribonucleotide Reductase. 2. Evidence for and Consequences of Blocked Electron Transfer in the W48F Variant

5. Rational Reprogramming of the R2 Subunit of Escherichia coli Ribonucleotide Reductase into a Self-Hydroxylating Monooxygenase

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