46 results on '"Zhu, Xiao-Qing"'
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2. Characteristic Activity Parameters of Electron Donors and Electron Acceptors
3. Kinetic Studies of Hantzsch Ester and Dihydrogen Donors Releasing Two Hydrogen Atoms in Acetonitrile
4. New Insights into the Actual H-Abstraction Activities of Important Oxygen and Nitrogen Free Radicals: Thermodynamics and Kinetics in Acetonitrile
5. Discovering and Evaluating the Reducing Abilities of Polar Alkanes and Related Family Members as Organic Reductants Using Thermodynamics
6. Thermodynamic Network Cards of Hantzsch Ester, Benzothiazoline, and Dihydrophenanthridine Releasing Two Hydrogen Atoms or Ions on 20 Elementary Steps
7. Correction to “Theoretical Prediction of Activation Free Energies of Various Hydride Self-Exchange Reactions in Acetonitrile at 298 K”
8. Thermodynamic Parameters of Elementary Steps for 3,5-Disubstituted 1,4-Dihydropyridines To Release Hydride Anions in Acetonitrile
9. New Insight into the Mechanism of NADH Model Oxidation by Metal Ions in Nonalkaline Media
10. Theoretical Prediction of Activation Free Energies of Various Hydride Self-Exchange Reactions in Acetonitrile at 298 K
11. Unusual Topological RNA Architecture with an Eight-Stranded Helical Fragment Containing A-, G-, and U-Tetrads
12. Prediction of Kinetic Isotope Effects for Various Hydride Transfer Reactions Using a New Kinetic Model
13. Determination and Comparison of Thermodynamic Driving Forces of Elementary Steps for the Reductions of Alkynes and the Corresponding Alkenes in Acetonitrile
14. Determination of Thermodynamic Affinities of Various Polar Olefins as Hydride, Hydrogen Atom, and Electron Acceptors in Acetonitrile
15. A Thermodynamic and Kinetic Study of Hydride Transfer of a Caffeine Derivative
16. Conversion and Origin of Normal and Abnormal Temperature Dependences of Kinetic Isotope Effect in Hydride Transfer Reactions
17. What Are the Differences between Ascorbic Acid and NADH as Hydride and Electron Sources in Vivo on Thermodynamics, Kinetics, and Mechanism?
18. Actual Structure, Thermodynamic Driving Force, and Mechanism of Benzofuranone-Typical Compounds as Antioxidants in Solution
19. Hydride Affinity Scale of Various Substituted Arylcarbeniums in Acetonitrile
20. Scales of Oxidation Potentials, pKa, and BDE of Various Hydroquinones and Catechols in DMSO
21. Accurate Estimation of the One-Electron Reduction Potentials of Various Substituted Quinones in DMSO and CH3CN
22. Thermodynamic Diagnosis of the Properties and Mechanism of Dihydropyridine-Type Compounds as Hydride Source in Acetonitrile with “Molecule ID Card”
23. Hydride, Hydrogen, Proton, and Electron Affinities of Imines and Their Reaction Intermediates in Acetonitrile and Construction of Thermodynamic Characteristic Graphs (TCGs) of Imines as a “Molecule ID Card”
24. Establishment of the C−NO Bond Dissociation Energy Scale in Solution and Its Application in Analyzing the Trend of NO Transfer from C-Nitroso Compound to Thiols
25. Hydride Affinities of Cumulated, Isolated, and Conjugated Dienes in Acetonitrile
26. Driving Forces for the Mutual Conversions between Phenothiazines and Their Various Reaction Intermediates in Acetonitrile
27. Establishment of Heterolytic and Homolytic Y−NO2 Bond Dissociation Energy Scales of Nitro-Containing Compounds in Acetonitrile: Chemical Origin of NO2 Release and Capture
28. Hydride, Hydrogen Atom, Proton, and Electron Transfer Driving Forces of Various Five-Membered Heterocyclic Organic Hydrides and Their Reaction Intermediates in Acetonitrile
29. Theoretical Prediction of the Hydride Affinities of Variousp- ando-Quinones in DMSO
30. Mechanism and Driving Force of NO Transfer from S-Nitrosothiol to Cobalt(II) Porphyrin: A Detailed Thermodynamic and Kinetic Study
31. Negative Kinetic Temperature Effect on the Hydride Transfer from NADH Analogue BNAH to the Radical Cation of N-Benzylphenothiazine in Acetonitrile
32. Determination of N−NO Bond Dissociation Energies of N-Methyl-N-nitrosobenzenesulfonamides in Acetonitrile and Application in the Mechanism Analyses on NO Transfer
33. First Estimation of C4−H Bond Dissociation Energies of NADH and Its Radical Cation in Aqueous Solution [J. Am. Chem. Soc.2003,125, 15298−15299].
34. First Estimation of C4−H Bond Dissociation Energies of NADH and Its Radical Cation in Aqueous Solution
35. Polysiloxane-Supported NAD(P)H Model 1-Benzyl-1,4-dihydronicotinamide: Synthesis and Application in the Reduction of Activated Olefins
36. Dissociation Energies and Charge Distribution of the Co−NO Bond for Nitrosyl-α,β,γ,δ-tetraphenylporphinatocobalt(II) and Nitrosyl-α,β,γ,δ-tetraphenylporphinatocobalt(III) in Benzonitrile Solution
37. An Old but Simple and Efficient Method to Elucidate the Oxidation Mechanism of NAD(P)H Model 1-Aryl-1,4-dihydronicotinamides by Cations 2-Methyl-5-nitroisoquinolium, Tropylium, and Xanthylium in Aqueous Solution
38. Application of NAD(P)H Model Hantzsch 1,4-Dihydropyridine as a Mild Reducing Agent in Preparation of Cyclo Compounds
39. Mechanisms of the Oxidations of NAD(P)H Model Hantzsch 1,4-Dihydropyridines by Nitric Oxide and Its Donor N-Methyl-N-nitrosotoluene-p-sulfonamide
40. N−NO Bond Dissociation Energies of N-Nitroso Diphenylamine Derivatives (Or Analogues) and Their Radical Anions: Implications for the Effect of Reductive Electron Transfer on N−NO Bond Activation and for the Mechanisms of NO Transfer to Nitranions
41. Heterolytic and Homolytic N−H Bond Dissociation Energies of 4-Substituted Hantzsch 2,6-Dimethyl-1,4-dihydropyridines and the Effect of One-Electron Transfer on the N−H Bond Activation
42. The First O−NO Bond Energy Scale in Solution: Heterolytic and Homolytic Cleavage Enthalpies of O-Nitrosyl Carboxylate Compounds
43. A Remarkable Kinetic Isotope Effect in One-Electron Transfer from 1-Benzyl-1,4-dihydronicotinamide
44. Which Hydrogen Atom Is First Transferred in the NAD(P)H Model Hantzsch Ester Mediated Reactions via One-Step and Multistep Hydride Transfer?
45. Is NO (Nitric Oxide) an Electron Acceptor or an Electrophile? A Detailed Thermodynamic Investigation on the Mechanisms of NO-Initiated Reactions with 3,6-Dibromocarbazolide Anion and Related Carbanion
46. Carbanion: The First Example To Generate Thermodynamically Unfavorable 9-(Dicyanomethyl)fluorenide Anion
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