✦ LIBER ✦

New arylhydrazones of β-diketones and their optical and thermal properties

✍ Scribed by Zhen Ma; Abel M. Maharramov; Ismayil A. Aliyev; Irada N. Aliyeva; Maximilian N. Kopylovich; Gunel I. Amanullayeva; Kamran T. Mahmudov; Armando J.L. Pombeiro

Book ID: 113806346
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 416 KB
Volume: 1019
Category: Article
ISSN: 0022-2860
DOI: 10.1016/j.molstruc.2012.03.054

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and thermal properties of some

Synthesis and thermal properties of some lithium β-diketonates

✍ E. S. Filatov; P. A. Stabnikov; P. P. Semyannikov; S. V. Trubin; I. K. Igumenov 📂 Article 📅 2006 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 189 KB

Praseodymium β-diketonates and luminesce

Praseodymium β-diketonates and luminescence properties of their solutions

✍ S. B. Meshkova; A. V. Kiriak; Z. M. Topilova; A. M. Andrianov 📂 Article 📅 2007 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 211 KB

Thermal properties of hafnium(IV) and zi

Thermal properties of hafnium(IV) and zirconium(IV) β-diketonates

✍ Ksenia V. Zherikova; Natalia B. Morozova; Ludmila N. Zelenina; S. V. Sysoev; Tam 📂 Article 📅 2008 🏛 Springer Netherlands 🌐 English ⚖ 224 KB

Role of tautomerism and solvatochromism

Role of tautomerism and solvatochromism in UV–VIS spectra of arylhydrazones of β-diketones

✍ Wojciech Kuznik; Maximilian N. Kopylovich; Gunel I. Amanullayeva; Armando J.L. P 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 923 KB

Structural and thermal properties of thr

Structural and thermal properties of three cyano-substituted azoderivatives of β-diketones

✍ Kamran T. Mahmudov; Maximilian N. Kopylovich; Konstantin V. Luzyanin; Archana Mi 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 478 KB

Tautomeric and conformational properties

Tautomeric and conformational properties of β-diketones

✍ Natalya V. Belova; Valeriy V. Sliznev; Heinz Oberhammer; Georgiy V. Girichev 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 582 KB

Available literature data about keto-enol equilibrium in b-diketones with different substituents in b-positions (R1C(O)-CH 2 -C(O)R2) has been analyzed. It was concluded that substituents from group I (R = H, CH 3 , CF 3 , C(CH3) 3 ) strongly favour the enol tautomer, whereas substituents from group