Regioselective synthesis, isomerisation, oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers
Bisguaiacol F (BGF), a potentially safer and renewable bisphenol A (BPA) replacement made from lignin-derivable vanillyl alcohol ( p -VA), is a promising building block for future aromatic biopolymers. Unfortunately, like BPA synthesis, this electrophilic condensation reaction is also prone to regio...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2019-12, Vol.21 (24), p.6622-6633 |
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creator | Koelewijn, Steven-Friso Ruijten, Dieter Trullemans, Laura Renders, Tom Van Puyvelde, Peter Witters, Hilda Sels, Bert F |
description | Bisguaiacol F (BGF), a potentially safer and renewable bisphenol A (BPA) replacement made from lignin-derivable vanillyl alcohol (
p
-VA), is a promising building block for future aromatic biopolymers. Unfortunately, like BPA synthesis, this electrophilic condensation reaction is also prone to regioselectivity issues, giving rise to
m
,
p
- and
o
,
p
-BGF byproducts. In this work, the hitherto unconsidered influence of
m
,
p
-BGF,
viz
. the main isomeric byproduct of
p
,
p
-BGF synthesis, on the physicochemical properties of poly(BGF carbonate) (BGF-PC) was systematically investigated by random copolymerisation with different fractions of pure
m
,
p
-BGF (25, 50 and 75 wt%). To do so, the elusive
m
,
p
-isomer was made in unparalleled regioselectivity (72%) by alkylation condensation of isovanillyl alcohol (
m
-VA) with guaiacol. Surprisingly, no isomeric scrambling due to acid-catalysed isomerisation was encountered for pure BGF isomers, which strongly facilitates their synthesis in contrast to petrochemical bisphenol F (BPF). Furthermore, to ensure safer chemical design, an
in vitro
human oestrogen receptor (hER) transactivation assay was performed. Both pure
m
,
p
- and
p
,
p
-BGF displayed a significantly reduced oestrogenic potency (426457 times lower affinity than BPA) and oestrogenic efficacy (3950% of BPA's maximum induction). Interestingly, mutual comparison between
p
,
p
-BPF and
p
,
p
-BGF reveals and proves for the first time the direct link between
ortho
-methoxy substitution and reduced
in vitro
oestrogenic activity (for transactivation of hER). In contrast to
o
,
p
-BPA,
viz
. the main byproduct of
p
,
p
-BPA synthesis,
m
,
p
-BGF was proven suitable for utilization in thermoplastics, thereby avoiding time-consuming and labour-intensive (re)crystallizations to obtain regioisomerically pure
p
,
p
-BGF.
Biobased
ortho
-methoxy groups ameliorate classic bisphenol chemistry in terms of synthesis, safety and processing; bisguaiacol F is used as a test case. |
doi_str_mv | 10.1039/c9gc02619c |
format | Article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c9gc02619c</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c9gc02619c</sourcerecordid><originalsourceid>FETCH-rsc_primary_c9gc02619c3</originalsourceid><addsrcrecordid>eNqFj02LwkAQRAdR8GO9eBf66EKyO5OESK7KRs_iXWbHNrbEdJgehfx7EWQ97qke1KOglJoZ_WV0Wny7onI6yU3hempksjyNi2Sp-3-cJ0M1Frlobcwyz0bK77AiFqzRBbojSNeEMwpJBCR8RU9iA3ETAaMEzxU25MA-ZQpdBLY5guOW6-7tAp_gl6S6WbKOayhhsdqUn69B-VCDk60Fp6-cqHn5s19vYy_u0Hq6Wt8d3kfS__oH3cROBA</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Regioselective synthesis, isomerisation, oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Koelewijn, Steven-Friso ; Ruijten, Dieter ; Trullemans, Laura ; Renders, Tom ; Van Puyvelde, Peter ; Witters, Hilda ; Sels, Bert F</creator><creatorcontrib>Koelewijn, Steven-Friso ; Ruijten, Dieter ; Trullemans, Laura ; Renders, Tom ; Van Puyvelde, Peter ; Witters, Hilda ; Sels, Bert F</creatorcontrib><description>Bisguaiacol F (BGF), a potentially safer and renewable bisphenol A (BPA) replacement made from lignin-derivable vanillyl alcohol (
p
-VA), is a promising building block for future aromatic biopolymers. Unfortunately, like BPA synthesis, this electrophilic condensation reaction is also prone to regioselectivity issues, giving rise to
m
,
p
- and
o
,
p
-BGF byproducts. In this work, the hitherto unconsidered influence of
m
,
p
-BGF,
viz
. the main isomeric byproduct of
p
,
p
-BGF synthesis, on the physicochemical properties of poly(BGF carbonate) (BGF-PC) was systematically investigated by random copolymerisation with different fractions of pure
m
,
p
-BGF (25, 50 and 75 wt%). To do so, the elusive
m
,
p
-isomer was made in unparalleled regioselectivity (72%) by alkylation condensation of isovanillyl alcohol (
m
-VA) with guaiacol. Surprisingly, no isomeric scrambling due to acid-catalysed isomerisation was encountered for pure BGF isomers, which strongly facilitates their synthesis in contrast to petrochemical bisphenol F (BPF). Furthermore, to ensure safer chemical design, an
in vitro
human oestrogen receptor (hER) transactivation assay was performed. Both pure
m
,
p
- and
p
,
p
-BGF displayed a significantly reduced oestrogenic potency (426457 times lower affinity than BPA) and oestrogenic efficacy (3950% of BPA's maximum induction). Interestingly, mutual comparison between
p
,
p
-BPF and
p
,
p
-BGF reveals and proves for the first time the direct link between
ortho
-methoxy substitution and reduced
in vitro
oestrogenic activity (for transactivation of hER). In contrast to
o
,
p
-BPA,
viz
. the main byproduct of
p
,
p
-BPA synthesis,
m
,
p
-BGF was proven suitable for utilization in thermoplastics, thereby avoiding time-consuming and labour-intensive (re)crystallizations to obtain regioisomerically pure
p
,
p
-BGF.
Biobased
ortho
-methoxy groups ameliorate classic bisphenol chemistry in terms of synthesis, safety and processing; bisguaiacol F is used as a test case.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c9gc02619c</identifier><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2019-12, Vol.21 (24), p.6622-6633</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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>Koelewijn, Steven-Friso</creatorcontrib><creatorcontrib>Ruijten, Dieter</creatorcontrib><creatorcontrib>Trullemans, Laura</creatorcontrib><creatorcontrib>Renders, Tom</creatorcontrib><creatorcontrib>Van Puyvelde, Peter</creatorcontrib><creatorcontrib>Witters, Hilda</creatorcontrib><creatorcontrib>Sels, Bert F</creatorcontrib><title>Regioselective synthesis, isomerisation, oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>Bisguaiacol F (BGF), a potentially safer and renewable bisphenol A (BPA) replacement made from lignin-derivable vanillyl alcohol (
p
-VA), is a promising building block for future aromatic biopolymers. Unfortunately, like BPA synthesis, this electrophilic condensation reaction is also prone to regioselectivity issues, giving rise to
m
,
p
- and
o
,
p
-BGF byproducts. In this work, the hitherto unconsidered influence of
m
,
p
-BGF,
viz
. the main isomeric byproduct of
p
,
p
-BGF synthesis, on the physicochemical properties of poly(BGF carbonate) (BGF-PC) was systematically investigated by random copolymerisation with different fractions of pure
m
,
p
-BGF (25, 50 and 75 wt%). To do so, the elusive
m
,
p
-isomer was made in unparalleled regioselectivity (72%) by alkylation condensation of isovanillyl alcohol (
m
-VA) with guaiacol. Surprisingly, no isomeric scrambling due to acid-catalysed isomerisation was encountered for pure BGF isomers, which strongly facilitates their synthesis in contrast to petrochemical bisphenol F (BPF). Furthermore, to ensure safer chemical design, an
in vitro
human oestrogen receptor (hER) transactivation assay was performed. Both pure
m
,
p
- and
p
,
p
-BGF displayed a significantly reduced oestrogenic potency (426457 times lower affinity than BPA) and oestrogenic efficacy (3950% of BPA's maximum induction). Interestingly, mutual comparison between
p
,
p
-BPF and
p
,
p
-BGF reveals and proves for the first time the direct link between
ortho
-methoxy substitution and reduced
in vitro
oestrogenic activity (for transactivation of hER). In contrast to
o
,
p
-BPA,
viz
. the main byproduct of
p
,
p
-BPA synthesis,
m
,
p
-BGF was proven suitable for utilization in thermoplastics, thereby avoiding time-consuming and labour-intensive (re)crystallizations to obtain regioisomerically pure
p
,
p
-BGF.
Biobased
ortho
-methoxy groups ameliorate classic bisphenol chemistry in terms of synthesis, safety and processing; bisguaiacol F is used as a test case.</description><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj02LwkAQRAdR8GO9eBf66EKyO5OESK7KRs_iXWbHNrbEdJgehfx7EWQ97qke1KOglJoZ_WV0Wny7onI6yU3hempksjyNi2Sp-3-cJ0M1Frlobcwyz0bK77AiFqzRBbojSNeEMwpJBCR8RU9iA3ETAaMEzxU25MA-ZQpdBLY5guOW6-7tAp_gl6S6WbKOayhhsdqUn69B-VCDk60Fp6-cqHn5s19vYy_u0Hq6Wt8d3kfS__oH3cROBA</recordid><startdate>20191210</startdate><enddate>20191210</enddate><creator>Koelewijn, Steven-Friso</creator><creator>Ruijten, Dieter</creator><creator>Trullemans, Laura</creator><creator>Renders, Tom</creator><creator>Van Puyvelde, Peter</creator><creator>Witters, Hilda</creator><creator>Sels, Bert F</creator><scope/></search><sort><creationdate>20191210</creationdate><title>Regioselective synthesis, isomerisation, oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers</title><author>Koelewijn, Steven-Friso ; Ruijten, Dieter ; Trullemans, Laura ; Renders, Tom ; Van Puyvelde, Peter ; Witters, Hilda ; Sels, Bert F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c9gc02619c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koelewijn, Steven-Friso</creatorcontrib><creatorcontrib>Ruijten, Dieter</creatorcontrib><creatorcontrib>Trullemans, Laura</creatorcontrib><creatorcontrib>Renders, Tom</creatorcontrib><creatorcontrib>Van Puyvelde, Peter</creatorcontrib><creatorcontrib>Witters, Hilda</creatorcontrib><creatorcontrib>Sels, Bert F</creatorcontrib><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koelewijn, Steven-Friso</au><au>Ruijten, Dieter</au><au>Trullemans, Laura</au><au>Renders, Tom</au><au>Van Puyvelde, Peter</au><au>Witters, Hilda</au><au>Sels, Bert F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regioselective synthesis, isomerisation, oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2019-12-10</date><risdate>2019</risdate><volume>21</volume><issue>24</issue><spage>6622</spage><epage>6633</epage><pages>6622-6633</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>Bisguaiacol F (BGF), a potentially safer and renewable bisphenol A (BPA) replacement made from lignin-derivable vanillyl alcohol (
p
-VA), is a promising building block for future aromatic biopolymers. Unfortunately, like BPA synthesis, this electrophilic condensation reaction is also prone to regioselectivity issues, giving rise to
m
,
p
- and
o
,
p
-BGF byproducts. In this work, the hitherto unconsidered influence of
m
,
p
-BGF,
viz
. the main isomeric byproduct of
p
,
p
-BGF synthesis, on the physicochemical properties of poly(BGF carbonate) (BGF-PC) was systematically investigated by random copolymerisation with different fractions of pure
m
,
p
-BGF (25, 50 and 75 wt%). To do so, the elusive
m
,
p
-isomer was made in unparalleled regioselectivity (72%) by alkylation condensation of isovanillyl alcohol (
m
-VA) with guaiacol. Surprisingly, no isomeric scrambling due to acid-catalysed isomerisation was encountered for pure BGF isomers, which strongly facilitates their synthesis in contrast to petrochemical bisphenol F (BPF). Furthermore, to ensure safer chemical design, an
in vitro
human oestrogen receptor (hER) transactivation assay was performed. Both pure
m
,
p
- and
p
,
p
-BGF displayed a significantly reduced oestrogenic potency (426457 times lower affinity than BPA) and oestrogenic efficacy (3950% of BPA's maximum induction). Interestingly, mutual comparison between
p
,
p
-BPF and
p
,
p
-BGF reveals and proves for the first time the direct link between
ortho
-methoxy substitution and reduced
in vitro
oestrogenic activity (for transactivation of hER). In contrast to
o
,
p
-BPA,
viz
. the main byproduct of
p
,
p
-BPA synthesis,
m
,
p
-BGF was proven suitable for utilization in thermoplastics, thereby avoiding time-consuming and labour-intensive (re)crystallizations to obtain regioisomerically pure
p
,
p
-BGF.
Biobased
ortho
-methoxy groups ameliorate classic bisphenol chemistry in terms of synthesis, safety and processing; bisguaiacol F is used as a test case.</abstract><doi>10.1039/c9gc02619c</doi><tpages>12</tpages></addata></record> |
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identifier | ISSN: 1463-9262 |
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recordid | cdi_rsc_primary_c9gc02619c |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Regioselective synthesis, isomerisation, oestrogenic activity, and copolymerisation of bisguaiacol F (BGF) isomers |
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