Статті в журналах з теми "Triazeide"
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Iglesias, Bernardo A., Manfredo Hörner, Henrique E. Toma, and Koiti Araki. "5-(1-(4-phenyl)-3-(4-nitrophenyl)triazene)-10,15,20-triphenylporphyrin: a new triazene-porphyrin dye and its spectroelectrochemical properties." Journal of Porphyrins and Phthalocyanines 16, no. 02 (February 2012): 200–209. http://dx.doi.org/10.1142/s1088424612004501.
Повний текст джерелаAlbertin, Gabriele, Stefano Antoniutti, Marco Bedin, Jesús Castro, and Soledad Garcia-Fontán. "Synthesis and Characterization of Triazenide and Triazene Complexes of Ruthenium and Osmium." Inorganic Chemistry 45, no. 9 (May 2006): 3816–25. http://dx.doi.org/10.1021/ic052063u.
Повний текст джерелаHartmann, Edmund, Raimund Schmid, and Joachim Strähle. "Synthese von zweikernigen Triazenido- und Pentaazadienidokomplexen des einwertigen Silbers. Kristallstruktur von [Ag(MeOC6H4N3C6H4OM e)]2· 2/3 Py, [Ag(MeOC6H4N5C6H4OMe)]2 und [Ag(EtOC6H4N5C6H4OEt)]2 · Py / Dimeric Triazenido and Pentaazadienido Complexes of Monovalent Silver. Synthesis and Structure of [Ag(MeOC6H4N3C6H4OM e)]2· 2/3 Pyridine, [Ag(MeOC6H4N5C6H4OMe)]2 und [Ag(EtOC6H4N5C6H4OEt)]2 · Pyridine." Zeitschrift für Naturforschung B 44, no. 7 (July 1, 1989): 778–85. http://dx.doi.org/10.1515/znb-1989-0710.
Повний текст джерелаHartmann, Edmund, and Joachim Strähle. "Synthese und Struktur von 1,3-Bis(4-trifluormethylphenyl)triazenido-Komplexen des Kupfer(I) und Silber(I) / Synthesis and Structure of 1,3-Bis(4-trifluormethylphenyl)triazenido Complexes of Copper(I) and Silver(I)." Zeitschrift für Naturforschung B 43, no. 7 (July 1, 1988): 818–24. http://dx.doi.org/10.1515/znb-1988-0706.
Повний текст джерелаLee, Wei-Tsung, Matthias Zeller, and Adriana Lugosan. "Bis(triazenide), tris(triazenide), and lantern-type of triazenide iron complexes: Synthesis and structural characterization." Inorganica Chimica Acta 477 (May 2018): 109–13. http://dx.doi.org/10.1016/j.ica.2018.02.014.
Повний текст джерелаMcKay, Alasdair I., and Marcus L. Cole. "Structural diversity in a homologous series of donor free alkali metal complexes bearing a sterically demanding triazenide." Dalton Transactions 48, no. 9 (2019): 2948–52. http://dx.doi.org/10.1039/c8dt04983a.
Повний текст джерелаGyton, Matthew R., Anthony R. Leverett, Marcus L. Cole, and Alasdair I. McKay. "Bulky bis(aryl)triazenides: just aspiring amidinates? A structural and spectroscopic study." Dalton Transactions 49, no. 17 (2020): 5653–61. http://dx.doi.org/10.1039/d0dt00285b.
Повний текст джерелаShupenyuk, V. I., S. V. Mamykin, T. N. Taras, M. P. Matkivskyi, O. P. Sabadakh, and O. M. Matkivskyi. "Structure and Morphology of Anthraquinone Triazene Films on Silicon Substrate." Фізика і хімія твердого тіла 21, no. 1 (March 29, 2020): 117–23. http://dx.doi.org/10.15330/pcss.21.1.117-123.
Повний текст джерелаLeverett, Anthony R., Vera Diachenko, Marcus L. Cole, and Alasdair I. McKay. "Kinetic stabilization of low-oxidation state and terminal hydrido main group metal complexes by a sterically demanding N,N′-bis(2,6-terphenyl)triazenide." Dalton Transactions 48, no. 35 (2019): 13197–204. http://dx.doi.org/10.1039/c9dt02562f.
Повний текст джерелаVaughan, Keith, Elizabeth Turner, and Hilary Jenkins. "1,2-Bis-(1-{3-pyridyl-}3-methyltriazen-3-yl)ethane: Synthesis and X-ray crystal structure." Canadian Journal of Chemistry 82, no. 3 (March 1, 2004): 448–53. http://dx.doi.org/10.1139/v03-213.
Повний текст джерелаHartmann, Edmund, and Joachim Strähle. "Synthese und Kristallstruktur von [l,3-Bis(4-ethoxyphenyl)triazenido]pyridino-silber(I), einem dimeren Komplex mit kurzem Silber-Silber-Kontakt / Synthesis and Crystal Structure of [1,3-Bis(4-ethoxyphenyl)triazenido]pyridino Silver(I), a Dimeric Complex with a Short Silver-Silver Contact." Zeitschrift für Naturforschung B 43, no. 5 (May 1, 1988): 525–28. http://dx.doi.org/10.1515/znb-1988-0506.
Повний текст джерелаMangawa, Shrawan Kumar, Chiranjeev Sharma, Ashawani kumar Singh, and Satish K. Awasthi. "Expedient and efficient one pot synthesis of trifluoroethyl ethers from metal free 2,4,6-tris-(2,2,2-trifluoro-ethoxy)-[1,3,5] triazene." RSC Advances 5, no. 44 (2015): 35042–45. http://dx.doi.org/10.1039/c5ra00618j.
Повний текст джерелаKalden, Diana, Sven Krieck, Helmar Görls, and Matthias Westerhausen. "1,3-Bis(2,4,6-trimethylphenyl)triazenides of potassium, magnesium, calcium, and strontium." Dalton Transactions 44, no. 17 (2015): 8089–99. http://dx.doi.org/10.1039/c5dt00595g.
Повний текст джерелаMpofu, Pamburayi, Polla Rouf, Nathan J. O'Brien, Urban Forsberg, and Henrik Pedersen. "Thermal atomic layer deposition of In2O3 thin films using a homoleptic indium triazenide precursor and water." Dalton Transactions 51, no. 12 (2022): 4712–19. http://dx.doi.org/10.1039/d1dt03748j.
Повний текст джерелаDoucet, Katherine G., Cory C. Pye, and Thomas G. Enright. "An exploratory ab initio study of the SN2 reaction of 1,3,3-trimethyltriazene with halide ions." Canadian Journal of Chemistry 85, no. 11 (November 1, 2007): 958–63. http://dx.doi.org/10.1139/v07-110.
Повний текст джерелаLi, Bin, Kevin Huse, Christoph Wölper, and Stephan Schulz. "Synthesis and reactivity of heteroleptic zinc(i) complexes toward heteroallenes." Chemical Communications 57, no. 100 (2021): 13692–95. http://dx.doi.org/10.1039/d1cc05617d.
Повний текст джерелаSeck, Insa, Samba F. Ndoye, Lalla A. Ba, Alioune Fall, Abdoulaye Diop, Ismaïla Ciss, Abda Ba, et al. "Access to a Library of 1,3-disubstituted-1,2,3-triazenes and Evaluation of their Antimicrobial Properties." Current Topics in Medicinal Chemistry 20, no. 9 (May 17, 2020): 713–19. http://dx.doi.org/10.2174/1568026620666200127143005.
Повний текст джерелаPye, Cory C., Keith Vaughan, and Julie F. Glister. "An ab initio study of conformations and sigmatropic shifts in triazene and its mono-, di-, and trimethyl derivatives." Canadian Journal of Chemistry 80, no. 5 (May 1, 2002): 447–54. http://dx.doi.org/10.1139/v02-049.
Повний текст джерелаDoucet, Katherine G., Julie F. Glister, and Cory C. Pye. "An ab initio study of model triazene-based anticancer agents." Canadian Journal of Chemistry 88, no. 8 (August 2010): 709–15. http://dx.doi.org/10.1139/v10-023.
Повний текст джерелаLerner, Hans-Wolfram, Inge Sänger, Kurt Polborn, Michael Bolte, and Matthias Wagner. "Synthese der Amide M[N(SiMetBu2)(SitBu3)] (M = Li, Na) durch N2-Eliminierung aus den Triazeniden M[tBu3SiNNNSiMetBu2] (M = Li, Na) / Synthesis of the Amides M[N(SiMetBu2)(SitBu3)] (M = Li, Na) by N2-Elimination Reaction of the Triazenides M[tBu3SiNNNSiMetBu2] (M= Li, Na)." Zeitschrift für Naturforschung B 62, no. 10 (October 1, 2007): 1285–90. http://dx.doi.org/10.1515/znb-2007-1009.
Повний текст джерелаMoser, Shasta Lee, and Keith Vaughan. "Synthesis and characterization of a series of 4-methyl-1-[2-aryl-1-diazenyl]-1,4-diazepanes and 1,4-di-[2-aryl-1-diazenyl]-1,4-diazepanes." Canadian Journal of Chemistry 82, no. 12 (December 1, 2004): 1725–35. http://dx.doi.org/10.1139/v04-153.
Повний текст джерелаAlexander, Sean G., Marcus L. Cole, Craig M. Forsyth, Samantha K. Furfari, and Kristina Konstas. "Bulky triazenide complexes of alumino- and gallohydrides." Dalton Transactions, no. 13 (2009): 2326. http://dx.doi.org/10.1039/b817397d.
Повний текст джерелаVirag, Andrej, Anton Meden, Marijan Kočevar, and Slovenko Polanc. "Synthesis and Characterization of New Triazenide Salts†." Journal of Organic Chemistry 71, no. 10 (May 2006): 4014–17. http://dx.doi.org/10.1021/jo060178p.
Повний текст джерелаAlaoui, K., Y. El Kacimi, M. Galai, H. Serrar, R. Touir, S. Kaya, C. Kaya, and M. Ebn Touhami. "New triazepine carboxylate derivatives: correlation between corrosion inhibition property and chemical structure." International Journal of Industrial Chemistry 11, no. 1 (January 4, 2020): 23–42. http://dx.doi.org/10.1007/s40090-019-00199-5.
Повний текст джерелаLu, Guan-Han, Tzu-Chia Huang, Hsiao-Chin Hsueh, Shin-Cherng Yang, Ting-Wei Cho та Ho-Hsuan Chou. "Novel N-transfer reagent for converting α-amino acid derivatives to α-diazo compounds". Chemical Communications 57, № 39 (2021): 4839–42. http://dx.doi.org/10.1039/d1cc01285a.
Повний текст джерелаLiu, Lang, Mengyao She, Jun Zhang, Zhaohui Wang, Hua Liu, Mi Tang, Ping Liu, Shengyong Zhang, and Jianli Li. "A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization." Green Chemistry 22, no. 10 (2020): 3111–16. http://dx.doi.org/10.1039/c9gc04328d.
Повний текст джерелаFesenko, Anastasia A., Mikhail S. Grigoriev, and Anatoly D. Shutalev. "A convenient stereoselective access to novel 1,2,4-triazepan-3-ones/thiones via reduction or reductive alkylation of 7-membered cyclic semicarbazones and thiosemicarbazones." Organic & Biomolecular Chemistry 16, no. 43 (2018): 8072–89. http://dx.doi.org/10.1039/c8ob01766b.
Повний текст джерелаAbdel-Razik, H. H. "Synthesis of 1,3,5-triazepine-2,4-dione, pyrrolo[3,4-f][1,3,5]triazepine-2,4-dione, pyridazino[4,5-f][1,3,5]triazepine and 1,3,5,7,9-pentazaheptaline derivatives." Arkivoc 2004, no. 1 (May 17, 2004): 71–78. http://dx.doi.org/10.3998/ark.5550190.0005.106.
Повний текст джерелаMohamed, Shaaban K., and A. M. Nour El-Din. "Solid State Photolysis of Triazene 1 -Oxides with Naphthols. Synthesis of Azo Dyes." Journal of Chemical Research 23, no. 8 (August 1999): 508–9. http://dx.doi.org/10.1177/174751989902300827.
Повний текст джерелаXu, Lijun, Zhubo Liu, Weipeng Dong, Jinyu Song, Maozhong Miao, Jianfeng Xu, and Hongjun Ren. "Copper-free arylation of 3,3-disubstituted allylic halides with triazene-softened aryl Grignard reagents." Organic & Biomolecular Chemistry 13, no. 22 (2015): 6333–37. http://dx.doi.org/10.1039/c5ob00594a.
Повний текст джерелаWang, Qi, Tian Lu, Chenbin Wang, Guijuan Fan, Hongquan Yin, and Fu-Xue Chen. "Synthesis of 5,5′-azoxybistetrazole via nitration and de-oxygen rearrangement of triazene." New J. Chem. 41, no. 20 (2017): 11512–16. http://dx.doi.org/10.1039/c7nj02724a.
Повний текст джерелаCartei, G., V. Ceschia, M. Casasola, T. Giraldi, A. Sibau, and M. Sanzari. "Triazene (DTIC) hepatotoxicity (HPT)." Melanoma Research 3, no. 1 (March 1993): 37. http://dx.doi.org/10.1097/00008390-199303000-00126.
Повний текст джерелаVassilev, Vassil, Svetlana Simova, and Blagoy Blagoev. "Triazene Derivatives of Cytisine." Archiv der Pharmazie 318, no. 7 (1985): 669–71. http://dx.doi.org/10.1002/ardp.19853180721.
Повний текст джерелаNevěčná, Taťjana, Oldřich Pytela, Miroslav Ludwig, and Jaromír Kaválek. "Solvent effects on kinetics and mechanism of acid-catalyzed decomposition of 1,3-bis(4-methylphenyl)triazene I. Reactions in alcohols." Collection of Czechoslovak Chemical Communications 55, no. 1 (1990): 147–55. http://dx.doi.org/10.1135/cccc19900147.
Повний текст джерелаLudwig, Miroslav, and Miriam Kabíčková. "Kinetics and Mechanism of Acid-Catalyzed Decomposition of 1,3-Bis(4-methylphenyl)triazene in Hexane-Organic Acid Medium." Collection of Czechoslovak Chemical Communications 61, no. 3 (1996): 355–63. http://dx.doi.org/10.1135/cccc19960355.
Повний текст джерелаAmiri, Nayereh, Mohammad K. Rofouei, and Jahan B. Ghasemi. "Multivariate optimization, preconcentration and determination of mercury ions with (1-(p-acetyl phenyl)-3-(o-methyl benzoate)) triazene in aqueous samples using ICP-AES." Analytical Methods 8, no. 5 (2016): 1111–19. http://dx.doi.org/10.1039/c5ay03169a.
Повний текст джерелаKaradayı, Nevzat, Şükriye Çakmak, Mustafa Odabaşoğlu, and Orhan Büyükgüngör. "1,3-Bis(4-methylphenyl)triazene, 1-(4-chlorophenyl)-3-(4-fluorophenyl)triazene and 1-(4-fluorophenyl)-3-(4-methylphenyl)triazene." Acta Crystallographica Section C Crystal Structure Communications 61, no. 5 (April 23, 2005): o303—o305. http://dx.doi.org/10.1107/s0108270105004373.
Повний текст джерелаAngulakshmi, N., R. Baby Dhanalakshmi, Murugavel Kathiresan, Yingke Zhou, and A. Manuel Stephan. "The suppression of lithium dendrites by a triazine-based porous organic polymer-laden PEO-based electrolyte and its application for all-solid-state lithium batteries." Materials Chemistry Frontiers 4, no. 3 (2020): 933–40. http://dx.doi.org/10.1039/c9qm00707e.
Повний текст джерелаVinduš, Denis, and Mark Niemeyer. "Hetero- and Homoleptic Magnesium Triazenides." Inorganics 5, no. 2 (May 1, 2017): 33. http://dx.doi.org/10.3390/inorganics5020033.
Повний текст джерелаBeweries, Torsten, Fabian Reiß, Julia Rothe, Axel Schulz, and Alexander Villinger. "Triazenido Complexes of Titanocene(III)." European Journal of Inorganic Chemistry 2019, no. 14 (April 4, 2019): 1993–98. http://dx.doi.org/10.1002/ejic.201801272.
Повний текст джерелаLeger, Claus-Dieter, and Gerhard Maas. "Dinuclear Ruthenium(I)Triazenide Complexes as Catalysts for Carbenoid Cyclopropanation Reactions." Zeitschrift für Naturforschung B 59, no. 5 (May 1, 2004): 573–78. http://dx.doi.org/10.1515/znb-2004-0516.
Повний текст джерелаMartins, Marcos A. P., Paulo R. S. Salbego, Guilherme A. de Moraes, Caroline R. Bender, Priscilla J. Zambiazi, Tainára Orlando, Anderson B. Pagliari, Clarissa P. Frizzo та Manfredo Hörner. "Understanding the crystalline formation of triazene N-oxides and the role of halogen⋯π interactions". CrystEngComm 20, № 1 (2018): 96–112. http://dx.doi.org/10.1039/c7ce02015e.
Повний текст джерелаAly, Ashraf A., Ahmed M. NourEl-Din, Mohsen A. M. Gomaa, and Magda S. Fahmi. "Rapid and Facile Synthesis of 4-Aryl-5-imino-3-phenyl-1H-naphtho[2,3-f]-1,2,4-triazepine-6,11-diones via the Reaction of Amidrazones with Dicyanonaphthoquinone." Zeitschrift für Naturforschung B 63, no. 2 (February 1, 2008): 223–28. http://dx.doi.org/10.1515/znb-2008-0217.
Повний текст джерелаLafrance, Ronald J., Hartford W. Manning, and Keith Vaughan. "Open-chain nitrogen compounds. Part XII. Methanolysis of 3-alkyl-3,4-dihydro-1,2,3-benzotriazin-4-ols: evidence for ring-chain tautomerism with the cytotoxic monoalkyltriazenes." Canadian Journal of Chemistry 65, no. 2 (February 1, 1987): 292–97. http://dx.doi.org/10.1139/v87-048.
Повний текст джерелаVaughan, Keith, Hartford W. Manning, Marcus P. Merrin, and Donald L. Hooper. "Open chain nitrogen compounds. Part XIII. 1-Aryl-3-arylthiomethyl-3-methyltriazenes and 3-(arylazo)-1,3-thiazolidines." Canadian Journal of Chemistry 66, no. 10 (October 1, 1988): 2487–91. http://dx.doi.org/10.1139/v88-391.
Повний текст джерелаWang, Qi, Fuqing Pang, Guilong Wang, Jinglun Huang, Fude Nie, and Fu-Xue Chen. "Pentazadiene: a high-nitrogen linkage in energetic materials." Chemical Communications 53, no. 15 (2017): 2327–30. http://dx.doi.org/10.1039/c6cc08179g.
Повний текст джерелаSoussi, Khaled, Shashank Mishra, Erwann Jeanneau, Jean-Marc M. Millet, and Stéphane Daniele. "Asymmetrically substituted triazenes as poor electron donor ligands in the precursor chemistry of iron(ii) for iron-based metallic and intermetallic nanocrystals." Dalton Transactions 46, no. 38 (2017): 13055–64. http://dx.doi.org/10.1039/c7dt02755a.
Повний текст джерелаConnelly, Neil G., Owen D. Hayward, Phimphaka Klangsinsirikul, and A. Guy Orpen. "Novel dicarbonyl and carbonylnitrosyl tris(µ-triazenide) dirhodium complexes." Journal of the Chemical Society, Dalton Transactions, no. 3 (December 17, 2001): 305–6. http://dx.doi.org/10.1039/b109972h.
Повний текст джерелаBardaji, Manuel, Nathan C. Brown, Aristides Christofides, and Neil G. Connelly. "Triazenide-bridged dirhodium complexes containing redox-active cyanomanganese ligands." Journal of the Chemical Society, Dalton Transactions, no. 12 (1996): 2511. http://dx.doi.org/10.1039/dt9960002511.
Повний текст джерелаPreusser, Silvio, Diana Kalden, Damian Bevern, Ansgar Oberheide, Helmar Görls, Wolfgang Imhof, Matthias Westerhausen, and Sven Krieck. "Potassium Salts of Asymmetrically Substituted Amidinates and a Triazenide." European Journal of Inorganic Chemistry 2019, no. 14 (March 21, 2019): 1970–78. http://dx.doi.org/10.1002/ejic.201900159.
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