Comparison of Thermodynamic Energies for Elementary Steps of Anionic Hydrides to Release Hydride Ions in Acetonitrile. Issue 43 (16th November 2022)
- Record Type:
- Journal Article
- Title:
- Comparison of Thermodynamic Energies for Elementary Steps of Anionic Hydrides to Release Hydride Ions in Acetonitrile. Issue 43 (16th November 2022)
- Main Title:
- Comparison of Thermodynamic Energies for Elementary Steps of Anionic Hydrides to Release Hydride Ions in Acetonitrile
- Authors:
- Fu, Yan‐Hua
Yang, Li‐Guo
Zhou, Zhong‐Yuan
Jia, Taixuan
Shen, Guang‐Bin
Zhu, Xiao‐Qing - Abstract:
- Abstract: In this work, six thermodynamic parameters of 10 anionic hydrides XH − ascorbic acid (iAscH − ), alcohol anions, imine anion, activated olefin anions and diene anions and their intermediates in hydride transfer process were researched. The hydride‐donating, hydrogen‐atom‐donating and election‐donating abilities of XH −, and the electron‐accepting abilities of X were also discussed. Two physical parameters of free radical XH⋅, homolytic Gibbs free energy to release hydrogen atom Δ G o HD (XH⋅), heterolytic Gibbs free energy to release proton Δ G o PD (XH⋅), were determined to evaluate the antioxidant ability and acidity of intermediate XH⋅ in thermodynamics. The structure‐activity relationship of XH −, XH⋅ and X were carefully discussed. It's easy to find that the hydride‐donating abilities of XH − are stronger than their neutral compounds XH2 ; except for iAscH − ; the hydride‐donating abilities of XH − are stronger than their hydrogen‐atom‐donating abilities; the hydrogen‐atom‐donating abilities of XH − are weaker than their intermediate radicals XH⋅; the unsaturated compounds X are easier to accept electrons than the anionic hydrides XH − to donate electrons. This paper plays an important role in determining the mechanism of anionic hydride to release hydride ion and provides a new idea for the design and synthesis of more active hydride, hydrogen and electron donors. Abstract : Thermodynamic energies of oxygen centred, nitrogen centred and carbon centred 10Abstract: In this work, six thermodynamic parameters of 10 anionic hydrides XH − ascorbic acid (iAscH − ), alcohol anions, imine anion, activated olefin anions and diene anions and their intermediates in hydride transfer process were researched. The hydride‐donating, hydrogen‐atom‐donating and election‐donating abilities of XH −, and the electron‐accepting abilities of X were also discussed. Two physical parameters of free radical XH⋅, homolytic Gibbs free energy to release hydrogen atom Δ G o HD (XH⋅), heterolytic Gibbs free energy to release proton Δ G o PD (XH⋅), were determined to evaluate the antioxidant ability and acidity of intermediate XH⋅ in thermodynamics. The structure‐activity relationship of XH −, XH⋅ and X were carefully discussed. It's easy to find that the hydride‐donating abilities of XH − are stronger than their neutral compounds XH2 ; except for iAscH − ; the hydride‐donating abilities of XH − are stronger than their hydrogen‐atom‐donating abilities; the hydrogen‐atom‐donating abilities of XH − are weaker than their intermediate radicals XH⋅; the unsaturated compounds X are easier to accept electrons than the anionic hydrides XH − to donate electrons. This paper plays an important role in determining the mechanism of anionic hydride to release hydride ion and provides a new idea for the design and synthesis of more active hydride, hydrogen and electron donors. Abstract : Thermodynamic energies of oxygen centred, nitrogen centred and carbon centred 10 anionic hydrides to release hydrides, hydrogen atom and electron on six elementary steps were researched. The structure‐activity relationship of XH −, XH⋅ and X were carefully discussed. … (more)
- Is Part Of:
- ChemistrySelect. Volume 7:Issue 43(2022)
- Journal:
- ChemistrySelect
- Issue:
- Volume 7:Issue 43(2022)
- Issue Display:
- Volume 7, Issue 43 (2022)
- Year:
- 2022
- Volume:
- 7
- Issue:
- 43
- Issue Sort Value:
- 2022-0007-0043-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-11-16
- Subjects:
- anionic hydride -- electron-donating -- hydride-donating -- hydrogen-atom-donating -- structure-activity relationship
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.202203626 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24349.xml