{"title":"TEOS Oligomers and Transesters Identified by GC-MS in the sol-gel Process. Operational Mass Spectral Libraries","authors":"V. Bădescu","doi":"10.37358/rc.22.3.8530","DOIUrl":null,"url":null,"abstract":"\nThe aim of this article is the presentation of new user mass spectral libraries created based on unambiguous assigning of the mass spectra of the tetraethoxysilane (TEOS) oligomers and transesters obtained in the sol-gel process. Gas-chromatography coupled with mass spectrometry (GC-MS) was used to unambiguous identification the TEOS oligomers and transesters obtained in the hydrolysis, condensation and transesterification, reactions of tetraethoxysilane in parental solvent (EtOH) and nonparental solvents (MeOH and n-PrOH). The author�s procedure for the interpretation of mass spectra of silicon alkoxides was applied for TEOS, TEOS dimer, methoxy-transesters, and TEOS cyclic tetramer. GC and MS arguments for unambiguous assigning of TEOS oligomers and transesters in the sol-gel process were presented. Experimental B/E and B/E(1-E)1/2 linked scans, accurate mass at high resolution and M+1, M+2 isotopic effects, applied in previous works, were used as MS arguments. The NBS mass spectral library run under the RSX-11-PLUS operating system was used to create new mass spectral libraries. In this article are presented three user mass spectral libraries codified: TRANSME0 for methoxy-transesters, PROPOXY1 for propoxy-transesters in the histogram plot and tabular format and ICECHIM6 (first 12 entries in histogram plot format) for TEOS oligomers in the parental solvent.\n","PeriodicalId":21296,"journal":{"name":"Revista de Chimie","volume":"40 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista de Chimie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37358/rc.22.3.8530","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Materials Science","Score":null,"Total":0}
引用次数: 0
Abstract
The aim of this article is the presentation of new user mass spectral libraries created based on unambiguous assigning of the mass spectra of the tetraethoxysilane (TEOS) oligomers and transesters obtained in the sol-gel process. Gas-chromatography coupled with mass spectrometry (GC-MS) was used to unambiguous identification the TEOS oligomers and transesters obtained in the hydrolysis, condensation and transesterification, reactions of tetraethoxysilane in parental solvent (EtOH) and nonparental solvents (MeOH and n-PrOH). The author�s procedure for the interpretation of mass spectra of silicon alkoxides was applied for TEOS, TEOS dimer, methoxy-transesters, and TEOS cyclic tetramer. GC and MS arguments for unambiguous assigning of TEOS oligomers and transesters in the sol-gel process were presented. Experimental B/E and B/E(1-E)1/2 linked scans, accurate mass at high resolution and M+1, M+2 isotopic effects, applied in previous works, were used as MS arguments. The NBS mass spectral library run under the RSX-11-PLUS operating system was used to create new mass spectral libraries. In this article are presented three user mass spectral libraries codified: TRANSME0 for methoxy-transesters, PROPOXY1 for propoxy-transesters in the histogram plot and tabular format and ICECHIM6 (first 12 entries in histogram plot format) for TEOS oligomers in the parental solvent.
期刊介绍:
Revista de Chimie publishes original scientific studies submitted by romanian and foreign researchers and offers worldwide recognition of articles in many countries enabling their review in the publications of other researchers.
Published articles are in various fields of research:
* Chemistry
* Petrochemistry
* Chemical engineering
* Process equipment
* Biotechnology
* Environment protection
* Marketing & Management
* Applications in medicine
* Dental medicine
* Pharmacy