Preparation of dimethoxyborane and analysis by Fourier transform infrared spectroscopy

Andreas Bernas; Birgitta Peltopakka; Päivi Mäki-Arvela; Kari Eränen; Tapio Salmi; Dmitry Yu. Murzin

doi:10.1163/156856707781749919

Preparation of dimethoxyborane and analysis by Fourier transform infrared spectroscopy

Andreas Bernas, Birgitta Peltopakka, Päivi Mäki-Arvela, Kari Eränen, Tapio Salmi, Dmitry Yu. Murzin^*

^*Korresponderande författare för detta arbete

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

3 Citeringar (Scopus)

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Dimethoxyborane was prepared by the reaction of trimethoxyboroxine, sodium borohydride and trimethyl borate in diethylene glycol dimethyl ether solvent at 70°C under atmospheric pressure followed by distillation to increase the purity and analyzed in liquid phase by FT-IR. The concentration of dimethoxyborane was identified by hydrolysis with water, which yields boric acid, methanol and hydrogen, whereas the generated hydrogen was analyzed by the mass detector of a volumetric flow apparatus. The FT-IR absorbance peak area showed a linear dependence on dimethoxyborane concentration in the wavenumber range 873 to 950 cm^-1 for samples with dimethoxyborane concentrations 0 to 6.2 wt% in trimethyl borate. Data fitting using the least square method gave an R ² value of 97%.

Originalspråk	Engelska
Sidor (från-till)	645-654
Antal sidor	10
Tidskrift	Research on Chemical Intermediates
Volym	33
Nummer	7
DOI	https://doi.org/10.1163/156856707781749919
Status	Publicerad - 2007
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

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@article{d92db044299d427387499a225fe433b7,

title = "Preparation of dimethoxyborane and analysis by Fourier transform infrared spectroscopy",

abstract = "Dimethoxyborane was prepared by the reaction of trimethoxyboroxine, sodium borohydride and trimethyl borate in diethylene glycol dimethyl ether solvent at 70°C under atmospheric pressure followed by distillation to increase the purity and analyzed in liquid phase by FT-IR. The concentration of dimethoxyborane was identified by hydrolysis with water, which yields boric acid, methanol and hydrogen, whereas the generated hydrogen was analyzed by the mass detector of a volumetric flow apparatus. The FT-IR absorbance peak area showed a linear dependence on dimethoxyborane concentration in the wavenumber range 873 to 950 cm-1 for samples with dimethoxyborane concentrations 0 to 6.2 wt% in trimethyl borate. Data fitting using the least square method gave an R 2 value of 97%.",

keywords = "Dimethoxyborane, FT-IR, Hydrolysis, Trimethylborate",

author = "Andreas Bernas and Birgitta Peltopakka and P{\"a}ivi M{\"a}ki-Arvela and Kari Er{\"a}nen and Tapio Salmi and Murzin, {Dmitry Yu.}",

note = "Funding Information: This work is part of the activities at the {\AA}bo Akademi Process Chemistry Centre within the Finnish Centre of Excellence Programme (2000–2011) by the Academy of Finland. Financial support from Finnish Chemicals Oy is gratefully acknowledged. Copyright: Copyright 2008 Elsevier B.V., All rights reserved.",

year = "2007",

doi = "10.1163/156856707781749919",

language = "English",

volume = "33",

pages = "645--654",

journal = "Research on Chemical Intermediates",

issn = "0922-6168",

publisher = "Springer",

number = "7",

}

TY - JOUR

T1 - Preparation of dimethoxyborane and analysis by Fourier transform infrared spectroscopy

AU - Bernas, Andreas

AU - Peltopakka, Birgitta

AU - Mäki-Arvela, Päivi

AU - Eränen, Kari

AU - Salmi, Tapio

AU - Murzin, Dmitry Yu.

N1 - Funding Information: This work is part of the activities at the Åbo Akademi Process Chemistry Centre within the Finnish Centre of Excellence Programme (2000–2011) by the Academy of Finland. Financial support from Finnish Chemicals Oy is gratefully acknowledged. Copyright: Copyright 2008 Elsevier B.V., All rights reserved.

PY - 2007

Y1 - 2007

N2 - Dimethoxyborane was prepared by the reaction of trimethoxyboroxine, sodium borohydride and trimethyl borate in diethylene glycol dimethyl ether solvent at 70°C under atmospheric pressure followed by distillation to increase the purity and analyzed in liquid phase by FT-IR. The concentration of dimethoxyborane was identified by hydrolysis with water, which yields boric acid, methanol and hydrogen, whereas the generated hydrogen was analyzed by the mass detector of a volumetric flow apparatus. The FT-IR absorbance peak area showed a linear dependence on dimethoxyborane concentration in the wavenumber range 873 to 950 cm-1 for samples with dimethoxyborane concentrations 0 to 6.2 wt% in trimethyl borate. Data fitting using the least square method gave an R 2 value of 97%.

AB - Dimethoxyborane was prepared by the reaction of trimethoxyboroxine, sodium borohydride and trimethyl borate in diethylene glycol dimethyl ether solvent at 70°C under atmospheric pressure followed by distillation to increase the purity and analyzed in liquid phase by FT-IR. The concentration of dimethoxyborane was identified by hydrolysis with water, which yields boric acid, methanol and hydrogen, whereas the generated hydrogen was analyzed by the mass detector of a volumetric flow apparatus. The FT-IR absorbance peak area showed a linear dependence on dimethoxyborane concentration in the wavenumber range 873 to 950 cm-1 for samples with dimethoxyborane concentrations 0 to 6.2 wt% in trimethyl borate. Data fitting using the least square method gave an R 2 value of 97%.

KW - Dimethoxyborane

KW - FT-IR

KW - Hydrolysis

KW - Trimethylborate

UR - http://www.scopus.com/inward/record.url?scp=34548409080&partnerID=8YFLogxK

U2 - 10.1163/156856707781749919

DO - 10.1163/156856707781749919

M3 - Article

AN - SCOPUS:34548409080

SN - 0922-6168

VL - 33

SP - 645

EP - 654

JO - Research on Chemical Intermediates

JF - Research on Chemical Intermediates

IS - 7

ER -

Preparation of dimethoxyborane and analysis by Fourier transform infrared spectroscopy

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