Loading…
Experimental and theoretical study on benzoic acid derivatives
Benzoic (BA), p-hydroxybenzoic (HBA), m-methoxybenzoic (MBA), vanillic (VA) and syringic (SGA) acids were studied using both experimental and theoretical tools. The vibrational (FT-IR, FT-Raman) and 1H and 13C NMR spectra of benzoic acid derivatives were recorded. Characteristic shifts and changes i...
Saved in:
Published in: | Journal of molecular structure 2013-07, Vol.1044, p.181-187 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c402t-a73e6b505628d702a611b9753915b00e56460e37bb1eb2eaa1cffa78f9cac38a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c402t-a73e6b505628d702a611b9753915b00e56460e37bb1eb2eaa1cffa78f9cac38a3 |
container_end_page | 187 |
container_issue | |
container_start_page | 181 |
container_title | Journal of molecular structure |
container_volume | 1044 |
creator | Świsłocka, R. Regulska, E. Samsonowicz, M. Lewandowski, W. |
description | Benzoic (BA), p-hydroxybenzoic (HBA), m-methoxybenzoic (MBA), vanillic (VA) and syringic (SGA) acids were studied using both experimental and theoretical tools. The vibrational (FT-IR, FT-Raman) and 1H and 13C NMR spectra of benzoic acid derivatives were recorded. Characteristic shifts and changes in intensities of bands along the studied series were observed. The changes of chemical shifts of protons (1H NMR) and carbons (13C NMR) in the series of studied compounds were observed too. Optimized geometrical structures of studied compounds were obtained by B3LYP method using 6-31++G**, 6-311+G** and 6-311++G** basis sets. Aromaticity indices, atomic charges, dipole moments and energies were calculated. The theoretical chemical shifts in 1H and 13C NMR spectra and theoretical wavenumbers and intensities of IR and Raman spectra were determined. The calculated parameters were compared to experimental characteristic of studied compounds. |
doi_str_mv | 10.1016/j.molstruc.2012.12.005 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1762047123</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022286012011556</els_id><sourcerecordid>1762047123</sourcerecordid><originalsourceid>FETCH-LOGICAL-c402t-a73e6b505628d702a611b9753915b00e56460e37bb1eb2eaa1cffa78f9cac38a3</originalsourceid><addsrcrecordid>eNqFkMFqGzEQhkVJoI7TV2j2mMs6M9JKWl9Cg0mTQqCHNmeh1c62MuuVK2lN3KevgtNz4Idh4Ptn4GPsM8IKAdXNdrULY8pxdisOyFclAPIDW2Cred0CNmdsAcB5zVsFH9lFSlsAwFJesNv7lz1Fv6Mp27GyU1_l3xQiZe_KnvLcH6swVR1Nf4N3lXW-r_pSONjsD5Qu2flgx0Sf3uaSPX-9_7l5rJ--P3zb3D3VrgGea6sFqU6CVLztNXCrELu1lmKNsgMgqRoFJHTXIXWcrEU3DFa3w9pZJ1orluz6dHcfw5-ZUjY7nxyNo50ozMmgVhwajVy8j0oUjVxzKQuqTqiLIaVIg9kXFTYeDYJ5dWu25r9b8-rWlBS3pXh1Kg42GPsr-mSefxRAFq-iEagL8eVEULFy8BRNcp4mR72P5LLpg3_vyT_FFI77</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1513459255</pqid></control><display><type>article</type><title>Experimental and theoretical study on benzoic acid derivatives</title><source>ScienceDirect Journals</source><creator>Świsłocka, R. ; Regulska, E. ; Samsonowicz, M. ; Lewandowski, W.</creator><creatorcontrib>Świsłocka, R. ; Regulska, E. ; Samsonowicz, M. ; Lewandowski, W.</creatorcontrib><description>Benzoic (BA), p-hydroxybenzoic (HBA), m-methoxybenzoic (MBA), vanillic (VA) and syringic (SGA) acids were studied using both experimental and theoretical tools. The vibrational (FT-IR, FT-Raman) and 1H and 13C NMR spectra of benzoic acid derivatives were recorded. Characteristic shifts and changes in intensities of bands along the studied series were observed. The changes of chemical shifts of protons (1H NMR) and carbons (13C NMR) in the series of studied compounds were observed too. Optimized geometrical structures of studied compounds were obtained by B3LYP method using 6-31++G**, 6-311+G** and 6-311++G** basis sets. Aromaticity indices, atomic charges, dipole moments and energies were calculated. The theoretical chemical shifts in 1H and 13C NMR spectra and theoretical wavenumbers and intensities of IR and Raman spectra were determined. The calculated parameters were compared to experimental characteristic of studied compounds.</description><identifier>ISSN: 0022-2860</identifier><identifier>EISSN: 1872-8014</identifier><identifier>DOI: 10.1016/j.molstruc.2012.12.005</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Bands ; Benzoic acid ; Carbon ; Derivatives ; Dipole moment ; Fourier transform infrared spectroscopy ; Mathematical analysis ; NMR ; Nuclear magnetic resonance ; nuclear magnetic resonance spectroscopy ; Phenolic acids ; protons ; Raman ; Spectra</subject><ispartof>Journal of molecular structure, 2013-07, Vol.1044, p.181-187</ispartof><rights>2012 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-a73e6b505628d702a611b9753915b00e56460e37bb1eb2eaa1cffa78f9cac38a3</citedby><cites>FETCH-LOGICAL-c402t-a73e6b505628d702a611b9753915b00e56460e37bb1eb2eaa1cffa78f9cac38a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Świsłocka, R.</creatorcontrib><creatorcontrib>Regulska, E.</creatorcontrib><creatorcontrib>Samsonowicz, M.</creatorcontrib><creatorcontrib>Lewandowski, W.</creatorcontrib><title>Experimental and theoretical study on benzoic acid derivatives</title><title>Journal of molecular structure</title><description>Benzoic (BA), p-hydroxybenzoic (HBA), m-methoxybenzoic (MBA), vanillic (VA) and syringic (SGA) acids were studied using both experimental and theoretical tools. The vibrational (FT-IR, FT-Raman) and 1H and 13C NMR spectra of benzoic acid derivatives were recorded. Characteristic shifts and changes in intensities of bands along the studied series were observed. The changes of chemical shifts of protons (1H NMR) and carbons (13C NMR) in the series of studied compounds were observed too. Optimized geometrical structures of studied compounds were obtained by B3LYP method using 6-31++G**, 6-311+G** and 6-311++G** basis sets. Aromaticity indices, atomic charges, dipole moments and energies were calculated. The theoretical chemical shifts in 1H and 13C NMR spectra and theoretical wavenumbers and intensities of IR and Raman spectra were determined. The calculated parameters were compared to experimental characteristic of studied compounds.</description><subject>Bands</subject><subject>Benzoic acid</subject><subject>Carbon</subject><subject>Derivatives</subject><subject>Dipole moment</subject><subject>Fourier transform infrared spectroscopy</subject><subject>Mathematical analysis</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>Phenolic acids</subject><subject>protons</subject><subject>Raman</subject><subject>Spectra</subject><issn>0022-2860</issn><issn>1872-8014</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkMFqGzEQhkVJoI7TV2j2mMs6M9JKWl9Cg0mTQqCHNmeh1c62MuuVK2lN3KevgtNz4Idh4Ptn4GPsM8IKAdXNdrULY8pxdisOyFclAPIDW2Cred0CNmdsAcB5zVsFH9lFSlsAwFJesNv7lz1Fv6Mp27GyU1_l3xQiZe_KnvLcH6swVR1Nf4N3lXW-r_pSONjsD5Qu2flgx0Sf3uaSPX-9_7l5rJ--P3zb3D3VrgGea6sFqU6CVLztNXCrELu1lmKNsgMgqRoFJHTXIXWcrEU3DFa3w9pZJ1orluz6dHcfw5-ZUjY7nxyNo50ozMmgVhwajVy8j0oUjVxzKQuqTqiLIaVIg9kXFTYeDYJ5dWu25r9b8-rWlBS3pXh1Kg42GPsr-mSefxRAFq-iEagL8eVEULFy8BRNcp4mR72P5LLpg3_vyT_FFI77</recordid><startdate>20130724</startdate><enddate>20130724</enddate><creator>Świsłocka, R.</creator><creator>Regulska, E.</creator><creator>Samsonowicz, M.</creator><creator>Lewandowski, W.</creator><general>Elsevier B.V</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20130724</creationdate><title>Experimental and theoretical study on benzoic acid derivatives</title><author>Świsłocka, R. ; Regulska, E. ; Samsonowicz, M. ; Lewandowski, W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-a73e6b505628d702a611b9753915b00e56460e37bb1eb2eaa1cffa78f9cac38a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Bands</topic><topic>Benzoic acid</topic><topic>Carbon</topic><topic>Derivatives</topic><topic>Dipole moment</topic><topic>Fourier transform infrared spectroscopy</topic><topic>Mathematical analysis</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>Phenolic acids</topic><topic>protons</topic><topic>Raman</topic><topic>Spectra</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Świsłocka, R.</creatorcontrib><creatorcontrib>Regulska, E.</creatorcontrib><creatorcontrib>Samsonowicz, M.</creatorcontrib><creatorcontrib>Lewandowski, W.</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of molecular structure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Świsłocka, R.</au><au>Regulska, E.</au><au>Samsonowicz, M.</au><au>Lewandowski, W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experimental and theoretical study on benzoic acid derivatives</atitle><jtitle>Journal of molecular structure</jtitle><date>2013-07-24</date><risdate>2013</risdate><volume>1044</volume><spage>181</spage><epage>187</epage><pages>181-187</pages><issn>0022-2860</issn><eissn>1872-8014</eissn><abstract>Benzoic (BA), p-hydroxybenzoic (HBA), m-methoxybenzoic (MBA), vanillic (VA) and syringic (SGA) acids were studied using both experimental and theoretical tools. The vibrational (FT-IR, FT-Raman) and 1H and 13C NMR spectra of benzoic acid derivatives were recorded. Characteristic shifts and changes in intensities of bands along the studied series were observed. The changes of chemical shifts of protons (1H NMR) and carbons (13C NMR) in the series of studied compounds were observed too. Optimized geometrical structures of studied compounds were obtained by B3LYP method using 6-31++G**, 6-311+G** and 6-311++G** basis sets. Aromaticity indices, atomic charges, dipole moments and energies were calculated. The theoretical chemical shifts in 1H and 13C NMR spectra and theoretical wavenumbers and intensities of IR and Raman spectra were determined. The calculated parameters were compared to experimental characteristic of studied compounds.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.molstruc.2012.12.005</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-2860 |
ispartof | Journal of molecular structure, 2013-07, Vol.1044, p.181-187 |
issn | 0022-2860 1872-8014 |
language | eng |
recordid | cdi_proquest_miscellaneous_1762047123 |
source | ScienceDirect Journals |
subjects | Bands Benzoic acid Carbon Derivatives Dipole moment Fourier transform infrared spectroscopy Mathematical analysis NMR Nuclear magnetic resonance nuclear magnetic resonance spectroscopy Phenolic acids protons Raman Spectra |
title | Experimental and theoretical study on benzoic acid derivatives |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T04%3A03%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Experimental%20and%20theoretical%20study%20on%20benzoic%20acid%20derivatives&rft.jtitle=Journal%20of%20molecular%20structure&rft.au=%C5%9Awis%C5%82ocka,%20R.&rft.date=2013-07-24&rft.volume=1044&rft.spage=181&rft.epage=187&rft.pages=181-187&rft.issn=0022-2860&rft.eissn=1872-8014&rft_id=info:doi/10.1016/j.molstruc.2012.12.005&rft_dat=%3Cproquest_cross%3E1762047123%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c402t-a73e6b505628d702a611b9753915b00e56460e37bb1eb2eaa1cffa78f9cac38a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1513459255&rft_id=info:pmid/&rfr_iscdi=true |