Loading…

Mild Synthesis of a Dimethoxy‐Terminated Siloxane through a Ring‐Opening Reaction

Alkoxy‐terminated siloxanes can be used as coupling agents to improve the properties of materials, and they are also widely used in organic synthesis. Herein, a method to synthesize a dimethoxy‐terminated siloxane by the ring‐opening reaction of 2,4,6‐trimethyl‐2,4,6‐trivinyl‐1,3,5,2,4,6‐trioxatrisi...

Full description

Saved in:
Bibliographic Details
Published in:ChemistrySelect (Weinheim) 2022-02, Vol.7 (7), p.n/a
Main Authors: Liang, Nianjie, Li, Qiaosheng, Ge, Mengyuan, Gu, Defa, Liu, Yuzhou
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c2447-bb6ea78ee2bcb85d7161cfceea7b5877fabe21ee4ae12d81037d8ce0b1a766f03
container_end_page n/a
container_issue 7
container_start_page
container_title ChemistrySelect (Weinheim)
container_volume 7
creator Liang, Nianjie
Li, Qiaosheng
Ge, Mengyuan
Gu, Defa
Liu, Yuzhou
description Alkoxy‐terminated siloxanes can be used as coupling agents to improve the properties of materials, and they are also widely used in organic synthesis. Herein, a method to synthesize a dimethoxy‐terminated siloxane by the ring‐opening reaction of 2,4,6‐trimethyl‐2,4,6‐trivinyl‐1,3,5,2,4,6‐trioxatrisilinane (D3‐Vi) and methanol under mild condition was reported. The reaction does not require strong acids, strong bases or transition metal catalysts. The structure of the product was confirmed by 1H‐NMR, 29Si‐NMR and mass spectrometry (MS). The Gibbs free energy change of the reaction under the implicit solvent model was calculated by density functional theory (DFT), which proved the feasibility of the reaction. The calculation discussed the two‐step mechanism of the ring‐opening reaction. One methanol attacked D3‐Vi to form a monomethoxy‐terminated product, and then another methanol attacked from the other side to form a dimethoxy‐terminated product. The calculated reaction rate constants of the reaction at different temperatures indicate that the reaction has a tunneling effect, especially at low temperatures. Considering the complex reaction of D3‐Vi and methanol explained why the calculated rate constants at low temperatures were large but the ring‐opening reaction could hardly occur. The mild synthesis can promote the application of alkoxy‐terminated silicones. A method for synthesizing a dimethoxy‐terminated siloxane with high yield under mild conditions was reported. The reaction did not require strong acids, strong bases and transition metal catalysts. DFT calculations revealed the reaction mechanism and the existence of tunneling effects.
doi_str_mv 10.1002/slct.202104617
format article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_slct_202104617</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>SLCT202104617</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2447-bb6ea78ee2bcb85d7161cfceea7b5877fabe21ee4ae12d81037d8ce0b1a766f03</originalsourceid><addsrcrecordid>eNqFkL1OwzAUhS0EElXpypwXSLDdxE5HFP4qBVVq09mynZvGKHGq2Ihm4xF4Rp6EVEXAxnSPrr5zhg-ha4IjgjG9cY32EcWU4JgRfoYmdM6SkCXx4vxPvkQz514wxoSljCZ8grbPpimDzWB9Dc64oKsCGdyZFnzdHYbP948C-tZY6WGkTNMdpIXA1333uqtHcm3sboRWe7BjCtYgtTedvUIXlWwczL7vFG0f7ovsKcxXj8vsNg81jWMeKsVA8hSAKq3SpOSEEV1pGJ8qSTmvpAJKAGIJhJYpwXNephqwIpIzVuH5FEWnXd13zvVQiX1vWtkPgmBx9CKOXsSPl7GwOBXeTAPDP7TY5Fnx2_0CWGBrPg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Mild Synthesis of a Dimethoxy‐Terminated Siloxane through a Ring‐Opening Reaction</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Liang, Nianjie ; Li, Qiaosheng ; Ge, Mengyuan ; Gu, Defa ; Liu, Yuzhou</creator><creatorcontrib>Liang, Nianjie ; Li, Qiaosheng ; Ge, Mengyuan ; Gu, Defa ; Liu, Yuzhou</creatorcontrib><description>Alkoxy‐terminated siloxanes can be used as coupling agents to improve the properties of materials, and they are also widely used in organic synthesis. Herein, a method to synthesize a dimethoxy‐terminated siloxane by the ring‐opening reaction of 2,4,6‐trimethyl‐2,4,6‐trivinyl‐1,3,5,2,4,6‐trioxatrisilinane (D3‐Vi) and methanol under mild condition was reported. The reaction does not require strong acids, strong bases or transition metal catalysts. The structure of the product was confirmed by 1H‐NMR, 29Si‐NMR and mass spectrometry (MS). The Gibbs free energy change of the reaction under the implicit solvent model was calculated by density functional theory (DFT), which proved the feasibility of the reaction. The calculation discussed the two‐step mechanism of the ring‐opening reaction. One methanol attacked D3‐Vi to form a monomethoxy‐terminated product, and then another methanol attacked from the other side to form a dimethoxy‐terminated product. The calculated reaction rate constants of the reaction at different temperatures indicate that the reaction has a tunneling effect, especially at low temperatures. Considering the complex reaction of D3‐Vi and methanol explained why the calculated rate constants at low temperatures were large but the ring‐opening reaction could hardly occur. The mild synthesis can promote the application of alkoxy‐terminated silicones. A method for synthesizing a dimethoxy‐terminated siloxane with high yield under mild conditions was reported. The reaction did not require strong acids, strong bases and transition metal catalysts. DFT calculations revealed the reaction mechanism and the existence of tunneling effects.</description><identifier>ISSN: 2365-6549</identifier><identifier>EISSN: 2365-6549</identifier><identifier>DOI: 10.1002/slct.202104617</identifier><language>eng</language><subject>Density functional calculations ; Dimethoxy-terminated ; Ring-opening ; Transition states ; Tunneling effect</subject><ispartof>ChemistrySelect (Weinheim), 2022-02, Vol.7 (7), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2447-bb6ea78ee2bcb85d7161cfceea7b5877fabe21ee4ae12d81037d8ce0b1a766f03</cites><orcidid>0000-0002-1109-7704</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Liang, Nianjie</creatorcontrib><creatorcontrib>Li, Qiaosheng</creatorcontrib><creatorcontrib>Ge, Mengyuan</creatorcontrib><creatorcontrib>Gu, Defa</creatorcontrib><creatorcontrib>Liu, Yuzhou</creatorcontrib><title>Mild Synthesis of a Dimethoxy‐Terminated Siloxane through a Ring‐Opening Reaction</title><title>ChemistrySelect (Weinheim)</title><description>Alkoxy‐terminated siloxanes can be used as coupling agents to improve the properties of materials, and they are also widely used in organic synthesis. Herein, a method to synthesize a dimethoxy‐terminated siloxane by the ring‐opening reaction of 2,4,6‐trimethyl‐2,4,6‐trivinyl‐1,3,5,2,4,6‐trioxatrisilinane (D3‐Vi) and methanol under mild condition was reported. The reaction does not require strong acids, strong bases or transition metal catalysts. The structure of the product was confirmed by 1H‐NMR, 29Si‐NMR and mass spectrometry (MS). The Gibbs free energy change of the reaction under the implicit solvent model was calculated by density functional theory (DFT), which proved the feasibility of the reaction. The calculation discussed the two‐step mechanism of the ring‐opening reaction. One methanol attacked D3‐Vi to form a monomethoxy‐terminated product, and then another methanol attacked from the other side to form a dimethoxy‐terminated product. The calculated reaction rate constants of the reaction at different temperatures indicate that the reaction has a tunneling effect, especially at low temperatures. Considering the complex reaction of D3‐Vi and methanol explained why the calculated rate constants at low temperatures were large but the ring‐opening reaction could hardly occur. The mild synthesis can promote the application of alkoxy‐terminated silicones. A method for synthesizing a dimethoxy‐terminated siloxane with high yield under mild conditions was reported. The reaction did not require strong acids, strong bases and transition metal catalysts. DFT calculations revealed the reaction mechanism and the existence of tunneling effects.</description><subject>Density functional calculations</subject><subject>Dimethoxy-terminated</subject><subject>Ring-opening</subject><subject>Transition states</subject><subject>Tunneling effect</subject><issn>2365-6549</issn><issn>2365-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkL1OwzAUhS0EElXpypwXSLDdxE5HFP4qBVVq09mynZvGKHGq2Ihm4xF4Rp6EVEXAxnSPrr5zhg-ha4IjgjG9cY32EcWU4JgRfoYmdM6SkCXx4vxPvkQz514wxoSljCZ8grbPpimDzWB9Dc64oKsCGdyZFnzdHYbP948C-tZY6WGkTNMdpIXA1333uqtHcm3sboRWe7BjCtYgtTedvUIXlWwczL7vFG0f7ovsKcxXj8vsNg81jWMeKsVA8hSAKq3SpOSEEV1pGJ8qSTmvpAJKAGIJhJYpwXNephqwIpIzVuH5FEWnXd13zvVQiX1vWtkPgmBx9CKOXsSPl7GwOBXeTAPDP7TY5Fnx2_0CWGBrPg</recordid><startdate>20220218</startdate><enddate>20220218</enddate><creator>Liang, Nianjie</creator><creator>Li, Qiaosheng</creator><creator>Ge, Mengyuan</creator><creator>Gu, Defa</creator><creator>Liu, Yuzhou</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-1109-7704</orcidid></search><sort><creationdate>20220218</creationdate><title>Mild Synthesis of a Dimethoxy‐Terminated Siloxane through a Ring‐Opening Reaction</title><author>Liang, Nianjie ; Li, Qiaosheng ; Ge, Mengyuan ; Gu, Defa ; Liu, Yuzhou</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2447-bb6ea78ee2bcb85d7161cfceea7b5877fabe21ee4ae12d81037d8ce0b1a766f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Density functional calculations</topic><topic>Dimethoxy-terminated</topic><topic>Ring-opening</topic><topic>Transition states</topic><topic>Tunneling effect</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liang, Nianjie</creatorcontrib><creatorcontrib>Li, Qiaosheng</creatorcontrib><creatorcontrib>Ge, Mengyuan</creatorcontrib><creatorcontrib>Gu, Defa</creatorcontrib><creatorcontrib>Liu, Yuzhou</creatorcontrib><collection>CrossRef</collection><jtitle>ChemistrySelect (Weinheim)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liang, Nianjie</au><au>Li, Qiaosheng</au><au>Ge, Mengyuan</au><au>Gu, Defa</au><au>Liu, Yuzhou</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mild Synthesis of a Dimethoxy‐Terminated Siloxane through a Ring‐Opening Reaction</atitle><jtitle>ChemistrySelect (Weinheim)</jtitle><date>2022-02-18</date><risdate>2022</risdate><volume>7</volume><issue>7</issue><epage>n/a</epage><issn>2365-6549</issn><eissn>2365-6549</eissn><abstract>Alkoxy‐terminated siloxanes can be used as coupling agents to improve the properties of materials, and they are also widely used in organic synthesis. Herein, a method to synthesize a dimethoxy‐terminated siloxane by the ring‐opening reaction of 2,4,6‐trimethyl‐2,4,6‐trivinyl‐1,3,5,2,4,6‐trioxatrisilinane (D3‐Vi) and methanol under mild condition was reported. The reaction does not require strong acids, strong bases or transition metal catalysts. The structure of the product was confirmed by 1H‐NMR, 29Si‐NMR and mass spectrometry (MS). The Gibbs free energy change of the reaction under the implicit solvent model was calculated by density functional theory (DFT), which proved the feasibility of the reaction. The calculation discussed the two‐step mechanism of the ring‐opening reaction. One methanol attacked D3‐Vi to form a monomethoxy‐terminated product, and then another methanol attacked from the other side to form a dimethoxy‐terminated product. The calculated reaction rate constants of the reaction at different temperatures indicate that the reaction has a tunneling effect, especially at low temperatures. Considering the complex reaction of D3‐Vi and methanol explained why the calculated rate constants at low temperatures were large but the ring‐opening reaction could hardly occur. The mild synthesis can promote the application of alkoxy‐terminated silicones. A method for synthesizing a dimethoxy‐terminated siloxane with high yield under mild conditions was reported. The reaction did not require strong acids, strong bases and transition metal catalysts. DFT calculations revealed the reaction mechanism and the existence of tunneling effects.</abstract><doi>10.1002/slct.202104617</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-1109-7704</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 2365-6549
ispartof ChemistrySelect (Weinheim), 2022-02, Vol.7 (7), p.n/a
issn 2365-6549
2365-6549
language eng
recordid cdi_crossref_primary_10_1002_slct_202104617
source Wiley-Blackwell Read & Publish Collection
subjects Density functional calculations
Dimethoxy-terminated
Ring-opening
Transition states
Tunneling effect
title Mild Synthesis of a Dimethoxy‐Terminated Siloxane through a Ring‐Opening Reaction
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T14%3A07%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mild%20Synthesis%20of%20a%20Dimethoxy%E2%80%90Terminated%20Siloxane%20through%20a%20Ring%E2%80%90Opening%20Reaction&rft.jtitle=ChemistrySelect%20(Weinheim)&rft.au=Liang,%20Nianjie&rft.date=2022-02-18&rft.volume=7&rft.issue=7&rft.epage=n/a&rft.issn=2365-6549&rft.eissn=2365-6549&rft_id=info:doi/10.1002/slct.202104617&rft_dat=%3Cwiley_cross%3ESLCT202104617%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2447-bb6ea78ee2bcb85d7161cfceea7b5877fabe21ee4ae12d81037d8ce0b1a766f03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true