Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Synthesis: Molecular Structure, Thermal-Calorimetric and Computational Analyses, of Three New Amine Borane Adducts

Title: Synthesis: Molecular Structure, Thermal-Calorimetric and Computational Analyses, of Three New Amine Borane Adducts
Authors: Kevin Turani-I-Belloto; Rodica Chiriac; François Toche; Eddy Petit; Pascal G. Yot; Johan G. Alauzun; Umit B. Demirci
Source: Molecules, Vol 28, Iss 3, p 1469 (2023)
Publisher Information: MDPI AG
Publication Year: 2023
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: adduct; amine borane; boranes; boron chemistry; dihydrogen bonds; Organic chemistry; QD241-441
Description: Cyclopropylamine borane C 3 H 5 NH 2 BH 3 (C3AB), 2-ethyl-1-hexylamine borane CH 3 (CH 2 ) 3 CH(C 2 H 5 )CH 2 NH 2 BH 3 (C2C6AB) and didodecylamine borane (C 12 H 25 ) 2 NHBH 3 ((C12)2AB) are three new amine borane adducts (ABAs). They are synthesized by reaction of the corresponding amines with a borane complex, the reaction being exothermic as shown by Calvet calorimetry. The successful synthesis of each has been demonstrated by FTIR, Raman and NMR. For instance, the 11 B NMR spectra show the presence of signals typical of the NBH 3 environment, thereby implying the formation of B–N bonds. The occurrence of dihydrogen bonds (DHBs) for each of the ABAs has been highlighted by DSC and FTIR, and supported by DFT calculations (via the Mulliken charges for example). When heated, the three ABAs behave differently: C3AB and C2C6AB decompose from 68 to 100 °C whereas (C12)2AB is relatively stable up to 173 °C. That means that these ABAs are not appropriate as hydrogen carriers, but the ‘most’ stable (C12)2AB could open perspectives for the synthesis of advanced materials.
Document Type: article in journal/newspaper
Language: English
Relation: https://www.mdpi.com/1420-3049/28/3/1469; https://doaj.org/toc/1420-3049; https://doaj.org/article/417994dda5bf468abc4afac8bd3d2f98
DOI: 10.3390/molecules28031469
Availability: https://doi.org/10.3390/molecules28031469; https://doaj.org/article/417994dda5bf468abc4afac8bd3d2f98
Accession Number: edsbas.5647146B
Database: BASE