My Hang V. Huynh
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
My Hang V. Huynh has a total of 48 co-authors. Here are the top co-authors by number of shared publications:
Peter S. White
Department of Chemistry, State University of New York at Buffalo, Buffalo, New York 14260, the Chemistry Division, C-SIC Group and the Dynamic Experimentation Division, DX-2: HE Science and Technology Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, and the Department of Chemistry, Gettysburg College, Gettysburg, Pennsylvania 17325
13 shared publications- Thomas J. Meyer
Associate Director for Strategic Research Los Alamos National Laboratory, MS A127 Los Alamos, NM 87545 (USA) Fax: (+1) 505‐667‐5450
12 shared publications - Michael A. Hiskey
Dynamic Experiment Division, DX‐2: Materials Dynamics Group, MS C920, Los Alamos National Laboratory, Los Alamos, NM 87545, USA, Fax: (+1) 505‐667‐0500
9 shared publications Donald L. Jameson
Dynamic Experimentation Division, DX-2: Materials Dynamics Group, MS C920, and The Associate Director for Strategic Research, MS A127, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, and Department of Chemistry, Gettysburg College, Gettysburg, Pennsylvania 17325
7 shared publicationsThomas J. Meyer
Dynamic Experimentation Division, DX-2: Materials Dynamics Group, MS C920, and The Associate Director for Strategic Research, MS A127, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, and Department of Chemistry, Gettysburg College, Gettysburg, Pennsylvania 17325
6 shared publicationsRichard Gilardi
Naval Research Laboratory, Laboratory for the Structure of Matter , Washington, D.C., USA
5 shared publications
Latest Publications
- 31 October 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (43) , 7089-7094
Tetraazapentalene Chemistry: Unexpected Intramolecular Electron Rearrangement Induced by Highly Reactive ψ‐Dinitroso Substituents
- 31 October 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (43) , 7089-7094
Tetraazapentalene Chemistry: Unexpected Intramolecular Electron Rearrangement Induced by Highly Reactive ψ‐Dinitroso Substituents
- 31 October 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (43) , 7251-7256
Tetraazapentalene Chemistry: Unexpected Intramolecular Electron Rearrangement Induced by Highly Reactive ψ‐Dinitroso Substituents
- 31 October 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (43) , 7251-7256
Tetraazapentalene Chemistry: Unexpected Intramolecular Electron Rearrangement Induced by Highly Reactive ψ‐Dinitroso Substituents
- Top Cited Papers
- 20 August 2005
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 127 (36) , 12537-12543
Synthesis, Characterization, and Energetic Properties of Diazido Heteroaromatic High-Nitrogen C−N Compound
The synthesis, characterization, and energetic properties of diazido heteroaromatic high-nitrogen C−N compound, 3,6-diazido-1,2,4,5-tetrazine (DiAT), are reported. Its normalized heat of formation (NΔHf), experimentally determined using an additive method, is shown to be the highest positive NΔHf compared to all other organic molecules. The unexpected azido-tetrazolo tautomerizations and irreversible tetrazolo transformation of DiAT are remarkable compared to all other polyazido heteroaromatic high-nitrogen C−N compounds, for example, 2,4,6-triazido-1,3,5-triazine; 4,4‘,6,6‘-tetra(azido)hydrazo-1,3,5-triazine; 4,4‘,6,6‘-tetra(azido)azo-1,3,5-triazine; and 2,5,8-tri(azido)-1,3,4,6,7,9,9b-heptaazaphenalene (heptazine).
- 20 August 2005
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 127 (36) , 12537-12543
Top Cited PapersSynthesis, Characterization, and Energetic Properties of Diazido Heteroaromatic High-Nitrogen C−N Compound
The synthesis, characterization, and energetic properties of diazido heteroaromatic high-nitrogen C−N compound, 3,6-diazido-1,2,4,5-tetrazine (DiAT), are reported. Its normalized heat of formation (NΔHf), experimentally determined using an additive method, is shown to be the highest positive NΔHf compared to all other organic molecules. The unexpected azido-tetrazolo tautomerizations and irreversible tetrazolo transformation of DiAT are remarkable compared to all other polyazido heteroaromatic high-nitrogen C−N compounds, for example, 2,4,6-triazido-1,3,5-triazine; 4,4‘,6,6‘-tetra(azido)hydrazo-1,3,5-triazine; 4,4‘,6,6‘-tetra(azido)azo-1,3,5-triazine; and 2,5,8-tri(azido)-1,3,4,6,7,9,9b-heptaazaphenalene (heptazine).
- 22 April 2005
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 44 (10) , 3657-3663
Iminic N-Bound Iminophosphorano versus Nitrilic N-Bound Iminophosphorano Os(IV) Complexes: A New Double Derivatization of the Nitrido Ligand
The reactions between trans-[OsIV(tpy)(Cl)2(NCN)] (1) and PPh3 and between trans-[OsIV(tpy)(Cl)2(NPPh3)]+ (2) and CN- provide new examples of double derivatization of the nitrido ligand in an Os(VI)−nitrido complex (OsVI⋮N). The nitrilic N-bound product from the first reaction, trans-[OsII(tpy)(Cl)2(NCNPPh3)] (3), is the coordination isomer of the first iminic N-bound product from the second reaction, trans-[OsII(tpy)(Cl)2(N(CN)(PPh3))] (4). In CH3CN at 45 °C, 4 undergoes isomerrization to 3 followed by solvolysis and release of (N-cyano)iminophosphorane, NCNPPh3. These reactions demonstrate new double derivatization reactions of the nitrido ligand in OsVI⋮N with its implied synthetic utility.
- 22 April 2005
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 44 (10) , 3657-3663
Iminic N-Bound Iminophosphorano versus Nitrilic N-Bound Iminophosphorano Os(IV) Complexes: A New Double Derivatization of the Nitrido Ligand
The reactions between trans-[OsIV(tpy)(Cl)2(NCN)] (1) and PPh3 and between trans-[OsIV(tpy)(Cl)2(NPPh3)]+ (2) and CN- provide new examples of double derivatization of the nitrido ligand in an Os(VI)−nitrido complex (OsVI⋮N). The nitrilic N-bound product from the first reaction, trans-[OsII(tpy)(Cl)2(NCNPPh3)] (3), is the coordination isomer of the first iminic N-bound product from the second reaction, trans-[OsII(tpy)(Cl)2(N(CN)(PPh3))] (4). In CH3CN at 45 °C, 4 undergoes isomerrization to 3 followed by solvolysis and release of (N-cyano)iminophosphorane, NCNPPh3. These reactions demonstrate new double derivatization reactions of the nitrido ligand in OsVI⋮N with its implied synthetic utility.
- 30 March 2005
- Published by Taylor & Francis in Journal of Energetic Materials
- Vol. 23 (1) , 27-32
Preparation and Explosive Properties of Tetraamminebis(3,5-Dinitro-1,2,4-Triazolato-N1)Copper(II)
The synthesis of tetraamminebis(3,5-dinitro-1,2,4-triazolato-N1)copper(II) is reported along with its physical and sensitivity properties as well as crystal structure. In addition, the detonation velocity and CJ pressure have been determined at 0.5 inch diameter.
- 30 March 2005
- Published by Taylor & Francis in Journal of Energetic Materials
- Vol. 23 (1) , 27-32
Preparation and Explosive Properties of Tetraamminebis(3,5-Dinitro-1,2,4-Triazolato-N1)Copper(II)
The synthesis of tetraamminebis(3,5-dinitro-1,2,4-triazolato-N1)copper(II) is reported along with its physical and sensitivity properties as well as crystal structure. In addition, the detonation velocity and CJ pressure have been determined at 0.5 inch diameter.
- 18 January 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (5) , 737-739
Preparation of Nitrogen‐Rich Nanolayered, Nanoclustered, and Nanodendritic Carbon Nitrides
- 18 January 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (5) , 737-739
Preparation of Nitrogen‐Rich Nanolayered, Nanoclustered, and Nanodendritic Carbon Nitrides
- 18 January 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (5) , 747-749
Preparation of Nitrogen‐Rich Nanolayered, Nanoclustered, and Nanodendritic Carbon Nitrides
- 18 January 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (5) , 747-749
Preparation of Nitrogen‐Rich Nanolayered, Nanoclustered, and Nanodendritic Carbon Nitrides
- 1 January 2005
- Published by Springer Nature in MRS Proceedings
- Vol. 896
Energetic Decomposition of High-Nitrogen Metal Complexes and the Formation of Low-Density Nano-Structured Metal Monoliths
- 1 January 2005
- Published by Springer Nature in MRS Proceedings
- Vol. 896
Energetic Decomposition of High-Nitrogen Metal Complexes and the Formation of Low-Density Nano-Structured Metal Monoliths
- Open Access
- 20 October 2004
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 43 (42) , 5658-5661
3,6‐Di(azido)‐1,2,4,5‐Tetrazine: A Precursor for the Preparation of Carbon Nanospheres and Nitrogen‐Rich Carbon Nitrides
- 20 October 2004
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 43 (42) , 5658-5661
Open Access3,6‐Di(azido)‐1,2,4,5‐Tetrazine: A Precursor for the Preparation of Carbon Nanospheres and Nitrogen‐Rich Carbon Nitrides
- 20 October 2004
- Published by Wiley in Angewandte Chemie
- Vol. 116 (42) , 5776-5779
3,6‐Di(azido)‐1,2,4,5‐Tetrazine: A Precursor for the Preparation of Carbon Nanospheres and Nitrogen‐Rich Carbon Nitrides
- 20 October 2004
- Published by Wiley in Angewandte Chemie
- Vol. 116 (42) , 5776-5779
3,6‐Di(azido)‐1,2,4,5‐Tetrazine: A Precursor for the Preparation of Carbon Nanospheres and Nitrogen‐Rich Carbon Nitrides