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SM ISO690:2012 MELNIK, E., KRAVTSOV, Victor, BACHINSKII, Sergey, ISHKOV, Yu., PAVLOVSKY, Victor, ANDRONATI, Sergei. Synthesis and structure of 3-(1-naphthylmethylene)-,3-(2-naphthylmethylene)-, 3-(9-anthrylmethylene)-, 3-(quinolin-5-ylmethylene)-, and 3-(quinoxalin-5-ylmethylene)-1,2-dihydro-3H-1,4-benzodiazepin-2-ones. In: Materials Science and Condensed Matter Physics, Ed. 9, 25-28 septembrie 2018, Chișinău. Chișinău, Republica Moldova: Institutul de Fizică Aplicată, 2018, Ediția 9, p. 153. |
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Materials Science and Condensed Matter Physics Ediția 9, 2018 |
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Conferința "International Conference on Materials Science and Condensed Matter Physics" 9, Chișinău, Moldova, 25-28 septembrie 2018 | |||||||
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CZU: 544+546+538.9 | |||||||
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The search on new candidates for selective ligands of benzodiazepine receptors, and potential analgesics, stimulate us to synthesize the naphthalide- and heteronaphthalide-1,4-benzodiazepines. Condensation of 1,4-benzodiazepin-2-one 1 with 1- and 2-naphthalene, 9-anthracene and a number of quinoline and quinoxaline carbaldehydes resulted in 3-substituted 1,4-benzodiazepin-2-ones 2- 10. The structure of compounds 2-10 was confirmed by mass spectrometry and 1H NMR spectroscopy, and for (3Z)-7-bromo-5-phenyl-3-(quinoxalin-5-ylmethylene)-1,3-dihydro-2H-1,4- benzodiazepin-2-one 10 also by the X-ray diffraction method. The compound 10 crystallizes in the triclinic P-1 space group, a=7.9689(6), b=10.8434(8), c=12.5840(9) Å; α=80.627(6), β=75.074(6), =81.439(6), V=1030.1(1) Å3, Z=2 with one molecule per asymmetric unit. The seven-membered benzodiazepine ring in the molecule has the boat conformation. The N(1)–H•••O=C(2)=2.893(4) Å hydrogen bonds unite the molecules into centrosymmetric dimer forming R22(8) supramolecular synthon. The double C2=O2, N4=C5, and C3=C12 bond distances are equal to 1.221 (3), 1.276 (3), and 1.342 (4) Å, respectively. The planar quinoxaline fragments of neighboring center-symmetry related molecules reside in parallel planes with interplanar separation 3.501 Å, nevertheless they do not revealed the pronounced stacking interaction: the shortest centroid•••centroid benzene/benzene and benzene/pyrazine distances equal 4.093 and 4.242 Å, respectively. The C-H•••N6= 3.397 Å interactions unite the dimeric associates in the chain along crystallographic axis c. |
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<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' xmlns='http://datacite.org/schema/kernel-3' xsi:schemaLocation='http://datacite.org/schema/kernel-3 http://schema.datacite.org/meta/kernel-3/metadata.xsd'> <creators> <creator> <creatorName>Melnic, E.I.</creatorName> <affiliation>Institutul de Fizică Aplicată, Moldova, Republica</affiliation> </creator> <creator> <creatorName>Kravţov, V.H.</creatorName> <affiliation>Institutul de Fizică Aplicată, Moldova, Republica</affiliation> </creator> <creator> <creatorName>Bachinskii, S.Y.</creatorName> <affiliation>Физико-химический институт им. А.В. Богатского НАНУ, Ucraina</affiliation> </creator> <creator> <creatorName>Ishkov, Y.V.</creatorName> <affiliation>Одесский национальный университет им.И.И.Мечникова, Ucraina</affiliation> </creator> <creator> <creatorName>Pavlovsky, V.I.</creatorName> <affiliation>Физико-химический институт им. А.В. Богатского НАНУ, Ucraina</affiliation> </creator> <creator> <creatorName>Andronati, S.A.</creatorName> <affiliation>Физико-химический институт им. А.В. Богатского НАНУ, Ucraina</affiliation> </creator> </creators> <titles> <title xml:lang='en'>Synthesis and structure of 3-(1-naphthylmethylene)-,3-(2-naphthylmethylene)-, 3-(9-anthrylmethylene)-, 3-(quinolin-5-ylmethylene)-, and 3-(quinoxalin-5-ylmethylene)-1,2-dihydro-3H-1,4-benzodiazepin-2-ones</title> </titles> <publisher>Instrumentul Bibliometric National</publisher> <publicationYear>2018</publicationYear> <relatedIdentifier relatedIdentifierType='ISBN' relationType='IsPartOf'></relatedIdentifier> <subjects> <subject schemeURI='http://udcdata.info/' subjectScheme='UDC'>544+546+538.9</subject> </subjects> <dates> <date dateType='Issued'>2018</date> </dates> <resourceType resourceTypeGeneral='Text'>Conference Paper</resourceType> <descriptions> <description xml:lang='en' descriptionType='Abstract'><p>The search on new candidates for selective ligands of benzodiazepine receptors, and potential analgesics, stimulate us to synthesize the naphthalide- and heteronaphthalide-1,4-benzodiazepines. Condensation of 1,4-benzodiazepin-2-one <strong>1 </strong>with 1- and 2-naphthalene, 9-anthracene and a number of quinoline and quinoxaline carbaldehydes resulted in 3-substituted 1,4-benzodiazepin-2-ones <strong>2- 10</strong>. The structure of compounds <strong>2-10 </strong>was confirmed by mass spectrometry and 1H NMR spectroscopy, and for (3Z)-7-bromo-5-phenyl-3-(quinoxalin-5-ylmethylene)-1,3-dihydro-2H-1,4- benzodiazepin-2-one <strong>10 </strong>also by the X-ray diffraction method. The compound <strong>10 </strong>crystallizes in the triclinic <em>P-1 </em>space group, <em>a</em>=7.9689(6), <em>b</em>=10.8434(8), <em>c</em>=12.5840(9) Å; α=80.627(6), <em>β</em>=75.074(6), =81.439(6), <em>V</em>=1030.1(1) Å3, Z=2 with one molecule per asymmetric unit. The seven-membered benzodiazepine ring in the molecule has the boat conformation. The N(1)–H•••O=C(2)=2.893(4) Å hydrogen bonds unite the molecules into centrosymmetric dimer forming R22(8) supramolecular synthon. The double C2=O2, N4=C5, and C3=C12 bond distances are equal to 1.221 (3), 1.276 (3), and 1.342 (4) Å, respectively. The planar quinoxaline fragments of neighboring center-symmetry related molecules reside in parallel planes with interplanar separation 3.501 Å, nevertheless they do not revealed the pronounced stacking interaction: the shortest centroid•••centroid benzene/benzene and benzene/pyrazine distances equal 4.093 and 4.242 Å, respectively. The C-H•••N6= 3.397 Å interactions unite the dimeric associates in the chain along crystallographic axis <em>c</em>. </p></description> </descriptions> <formats> <format>application/pdf</format> </formats> </resource>