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showing 10 items of 9912 documents
CCDC 2131009: Experimental Crystal Structure Determination
2022
Related Article: Braulio M. Puerta Lombardi, Ethan R. Pezoulas, Roope A. Suvinen, Alexander Harrison, Zachary S. Dubrawski, Benjamin S. Gelfand, Heikki M. Tuononen, Roland Roesler|2022|Chem.Commun.|58|6482|doi:10.1039/D2CC01476A
CCDC 741667: Experimental Crystal Structure Determination
2009
Related Article: J.Zhao, V.Bohmer, M.Bolte|2009|Acta Crystallogr.,Sect.E:Struct.Rep.Online|65|o1658|doi:10.1107/S1600536809023344
CCDC 854391: Experimental Crystal Structure Determination
2012
Related Article: B.Os'mialowski, E.Kolehmainen, R.Dobosz, R.Gawinecki, R.Kauppinen, A.Valkonen, J.Koivukorpi, K.Rissanen|2010|J.Phys.Chem.A|114|10421|doi:10.1021/jp1063116
CCDC 777363: Experimental Crystal Structure Determination
2012
Related Article: S.Ikonen, O.Jurcek, Z.Wimmer, P.Drasar, E.Kolehmainen|2012|J.Mol.Struct.|1011|25|doi:10.1016/j.molstruc.2011.12.016
CCDC 777360: Experimental Crystal Structure Determination
2012
Related Article: S.Ikonen, O.Jurcek, Z.Wimmer, P.Drasar, E.Kolehmainen|2012|J.Mol.Struct.|1011|25|doi:10.1016/j.molstruc.2011.12.016
Evaluation of the 2-Methoxyethanol as Entrainer in Ethanol–Water and 1-Propanol–Water Mixtures
2013
In this paper, 2-methoxyethanol (commercially known as methyl cellosolve) is proposed as a potential entrainer for extractive distillation processes involving water–alcohol mixtures. The two alcohols studied in this work are ethanol and 1-propanol. Thereby, isobaric vapor–liquid equilibrium (VLE) data at atmospheric pressure have been measured for the ternary systems ethanol + water + 2-methoxyethanol and 1-propanol + water + 2-methoxyethanol. Moreover, data of the binary systems formed by the 2-methoxyethanol and each of the other chemicals used (ethanol, water, 1-propanol) have been obtained. The well-known local composition models Wilson, UNIQUAC, and NRTL have been used to correlate bin…
Keggin heteropolyacid supported on BN and C3N4: Comparison between catalytic and photocatalytic alcohol dehydration
2020
The Keggin heteropolyacid (HPA), H3PW12O40 (PW12) has been supported on commercial boron nitride (BN) and two types of home prepared carbon nitride (C3N4). The supported PW12 was used in the gas-solid (photo)catalytic 2-propanol dehydration reaction to give propene at atmospheric pressure and temperatures in the range 70–120 °C and resulted more active than the pristine PW12. Reaction rate increased by increasing the temperature. Noticeably, the propene formation rate was higher by irradiating the catalytic system. The PW12/BN material resulted more active than PW12/C3N4. The acidity of the HPA cluster accounts for the catalytic role, whereas both the acidity and the redox properties of the…
ZrO2 Based materials as photocatalysts for 2-propanol oxidation by using UV and solar light irradiation and tests for CO2 reduction
2018
Abstract Bare ZrO2, Ce doped ZrO2 and Er doped ZrO2 samples have been prepared by a hydrothermal process and have been used as photocatalysts for 2-propanol oxidation reaction in gas solid regime. Moreover, some preliminary tests have been carried out for CO2 reduction. The samples were physico-chemically characterized and both bare and doped ZrO2 based materials resulted active for oxidation and reduction reactions by using UV and solar irradiation. The reactivity results have been correlated with the compositional, structural and morphological features of the photocatalysts.
CCDC 1440861: Experimental Crystal Structure Determination
2017
Related Article: Olga Schäfer, David Huesmann, Christian Muhl, Matthias Barz|2016|Chem.-Eur.J.|22|18085|doi:10.1002/chem.201604391
2-cinnamamido, 2-(3-phenylpropiolamido) and 2-(3-phenylpropanamido)benzamides: synthesis, antiproliferative activity and mechanism of action
2013
Several new 2-cinnamamido, 2-(3-phenylpropiolamido) and 2-(3-phenylpropanamido)benzamides were synthesized by stirring in pyridine the opportune acid chlorides with the appropriate anthranilamide derivatives. Some of the synthesized compounds were evaluated for their in vitro antiproliferative activity against a panel of 5 human cell lines (K562 human chronic myelogenous leukemia cells, MCF-7 breast cancer cells, HTC-116 and HT26 colon cancer cells and NCI H460 non-small cell lung cancer cells).