Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
ISSN: |
1573-9171
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Keywords: |
X-ray crystallographic analysis ; heterylamidine ; N-(1,2,4-triazol-5-yl)benzamidine ; N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
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Source: |
Springer Online Journal Archives 1860-2000
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Topics: |
Chemistry and Pharmacology
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Notes: |
Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2.
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Type of Medium: |
Electronic Resource
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URL: |
_version_ | 1798297499013742594 |
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autor | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. |
autorsonst | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. |
book_url | http://dx.doi.org/10.1007/BF00866590 |
datenlieferant | nat_lic_papers |
hauptsatz | hsatz_simple |
identnr | NLM192206842 |
iqvoc_descriptor_keyword | iqvoc_00000708:analysis |
issn | 1573-9171 |
journal_name | Russian chemical bulletin |
materialart | 1 |
notes | Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2. |
package_name | Springer |
publikationsjahr_anzeige | 1992 |
publikationsjahr_facette | 1992 |
publikationsjahr_intervall | 8009:1990-1994 |
publikationsjahr_sort | 1992 |
publisher | Springer |
reference | 41 (1992), S. 1079-1083 |
schlagwort | X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride |
search_space | articles |
shingle_author_1 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. |
shingle_author_2 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. |
shingle_author_3 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. |
shingle_author_4 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. |
shingle_catch_all_1 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2. 1573-9171 15739171 Springer |
shingle_catch_all_2 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2. 1573-9171 15739171 Springer |
shingle_catch_all_3 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2. 1573-9171 15739171 Springer |
shingle_catch_all_4 | Kurella, M. G. Vorontsova, L. G. Amamchyan, A. R. Dorokhov, V. A. Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride X-ray crystallographic analysis heterylamidine N-(1,2,4-triazol-5-yl)benzamidine N-(1,2,4-triazol-5-yl)benzamidine hydrochloride Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2. 1573-9171 15739171 Springer |
shingle_title_1 | Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride |
shingle_title_2 | Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride |
shingle_title_3 | Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride |
shingle_title_4 | Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride |
sigel_instance_filter | dkfz geomar wilbert ipn albert fhp |
source_archive | Springer Online Journal Archives 1860-2000 |
timestamp | 2024-05-06T10:08:57.675Z |
titel | Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride |
titel_suche | Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride |
topic | V |
uid | nat_lic_papers_NLM192206842 |