1995
DOI: 10.1016/0022-2860(95)08599-q
|View full text |Cite
|
Sign up to set email alerts
|

Molecular absorption spectra of dinitramide and its salts

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
5
0

Year Published

1996
1996
2005
2005

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 7 publications
(5 citation statements)
references
References 0 publications
0
5
0
Order By: Relevance
“…Ultraviolet (UV) characteristic bands of ADN in an aqueous solution are similar to those of ammonium nitrate, sodium nitrite (NaNO 2 ), and cyclotetramethylenetetranitramine (HMX) [2,16,17] in the wavelength ranges of 220-250 nm and 280-300 nm. Infrared and Raman spectra of ADN and other dinitramide salts reported by Shlyapochnikov et al [17][18][19] and Christe et al [20] show strong IR absorptions at 1526 cm −1 (asymmetric stretch of NO 2 in phase), 1181 cm −1 (symmetric stretch of NO 2 out of phase), 1025 cm −1 (asymmetric stretch of N 3 ), and 3255 cm −1 (NH + 4 ) and 1407 cm −1 (NH + 4 ). The large energy release in ADN combustion (∆H f = −35.8 kcal/mole) as compared to AN (∆H f = −78 kcal/mole) and AP (∆H f = −70.7 kcal/mole) is attributed to the higher heat of formation of ADN [21].…”
Section: Introductionmentioning
confidence: 98%
“…Ultraviolet (UV) characteristic bands of ADN in an aqueous solution are similar to those of ammonium nitrate, sodium nitrite (NaNO 2 ), and cyclotetramethylenetetranitramine (HMX) [2,16,17] in the wavelength ranges of 220-250 nm and 280-300 nm. Infrared and Raman spectra of ADN and other dinitramide salts reported by Shlyapochnikov et al [17][18][19] and Christe et al [20] show strong IR absorptions at 1526 cm −1 (asymmetric stretch of NO 2 in phase), 1181 cm −1 (symmetric stretch of NO 2 out of phase), 1025 cm −1 (asymmetric stretch of N 3 ), and 3255 cm −1 (NH + 4 ) and 1407 cm −1 (NH + 4 ). The large energy release in ADN combustion (∆H f = −35.8 kcal/mole) as compared to AN (∆H f = −78 kcal/mole) and AP (∆H f = −70.7 kcal/mole) is attributed to the higher heat of formation of ADN [21].…”
Section: Introductionmentioning
confidence: 98%
“…Thus the free acid, NH(NO 2 ) 2 , should be called dinitraminic acid. The dinitramide ion is a uniquely stable oxy anion of nitrogen and its salts are high oxygen density groupings that have been prepared with many different counterions, including the ammonium, lithium, potassium, and cesium salts which are the subject of this report.…”
Section: Introductionmentioning
confidence: 99%
“…Following the publication of our patents, Russian workers at the Zelinsky Institute in Moscow on the whole and at the LNPO Soyuz facility and at the Zelinsky Institute in Moscow presented accounts of their independent research on the synthesis and use of dinitraminic acid and dinitramide salts. ,,,,− …”
Section: Introduction and Backgroundmentioning
confidence: 99%
“…[15][16][17][18][19][20][21][22] Following the publication of our patents, Russian workers at the Zelinsky Institute in Moscow on the whole and at the LNPO Soyuz facility and at the Zelinsky Institute in Moscow presented accounts of their independent research on the synthesis and use of dinitraminic acid and dinitramide salts. 3,7,9,13, [23][24][25][26][27][28] The choice of names for dinitramide salts is based on an extension of the well-established nomenclature for nitramide. The free acid, HN(NO 2 ) 2 , should be named dinitraminic acid.…”
Section: Introductionmentioning
confidence: 99%