✦ LIBER ✦

Horizontal thermal structure of the mesosphere from observations of OH(8-3) band emissions

✍ Scribed by C.A. Tepley; R.G. Burnside; J.W. Meriwether Jr.

Publisher: Elsevier Science
Year: 1981
Tongue: English
Weight: 975 KB
Volume: 29
Category: Article
ISSN: 0032-0633
DOI: 10.1016/0032-0633(81)90129-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The first observation of6I →8S emission

The first observation of6I →8S emission from Eu2+ in KMgF3

✍ A. Ellens; A. Meijerink; G. Blasse 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 299 KB

Crystal structure of Mg2(OH)2CO3, deduce

Crystal structure of Mg2(OH)2CO3, deduced from the topotactic thermal decomposition of artinite

✍ J.R. Günter; H.R. Oswald 📂 Article 📅 1977 🏛 Elsevier Science 🌐 English ⚖ 371 KB

The abundance of CH3D in the atmosphere

The abundance of CH3D in the atmosphere of Titan, derived from 8- to 14-μm thermal emission

✍ Sang J. Kim; John Caldwell 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 694 KB

Ab Initio Structure Solution of BaFeO2.8

Ab Initio Structure Solution of BaFeO2.8−δ, a New Polytype in the System BaFeOy (2.5≤y≤3.0) Prepared from the Oxidative Thermal Decomposition of BaFe[(CN)5NO]·3H2O

✍ Marı&#x0301;a Inés Gómez; Gabriela Lucotti; Juana A. de Morán; Pedro J. Aymo 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 474 KB

BaFeO 2.8؊ with a crystal structure di4erent from any of those previously reported in the system BaFeO y (2.54y43.0) was prepared by a low-temperature method of synthesis, based on the oxidative thermal decomposition of BaFe[(CN) 5 NO] ' 3H 2 O. The structure was solved ab initio by high-resolution

Addition and Cyclization Reactions in th

Addition and Cyclization Reactions in the Thermal Conversion of Hydrocarbons with an Enyne Structure, 4. Formation and Rearrangements of Bicyclic C10H8 Aromatics from 1-Phenyl-1-buten-3-yne

✍ Schulz, Kathrin ;Hofmann, Jörg ;Zimmermann, Gerhard 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 524 KB

## Abstract The thermal conversion of 1‐phenyl‐1‐buten‐3‐yne (1) into the cycloisomerization products naphthalene (2), azulene (3), and 1‐methylene‐1__H__‐indene (4) has been studied at temperatures between 550 and 1000°C, a reaction time of approximately 0.3 s at 13 Torr (FVP) and at low partial p

ChemInform Abstract: Addition and Cycliz

ChemInform Abstract: Addition and Cyclization Reactions in the Thermal Conversion of Hydrocarbons with an Enyne Structure. Part 4. Formation and Rearrangements of Bicyclic C10H8 Aromatics from 1-Phenyl-1-buten-3-yne.

✍ K. SCHULZ; J. HOFMANN; G. ZIMMERMANN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views