Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation

The radical anion of di(2,6-diethylphenyl)stannylene (Ar 2Sn) has been generated by the electrochemical reduction of cyclotristannane cyclo-(Ar 2Sn) 3, and the electrochemical oxidation of cyclo-(Ar 2Sn) 3 resulted in Sn–Sn bond cleavage with the formation of the radical cation of tristannane.

Saved in:
Bibliographic Details
Published in:Mendeleev communications 2002, Vol.12 (4), p.125-126
Main Authors: Orlov, Ivan S., Moiseeva, Anna A., Butin, Kim P., Sita, Lawrence R., Egorov, Mikhail P., Nefedov, Oleg M.
Format: Article
Language:English
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-c294t-d1144c99663eda04c08ad770d67cca4763f2e9522fd5dee879e7c45855ee7bf33
cites cdi_FETCH-LOGICAL-c294t-d1144c99663eda04c08ad770d67cca4763f2e9522fd5dee879e7c45855ee7bf33
container_end_page 126
container_issue 4
container_start_page 125
container_title Mendeleev communications
container_volume 12
creator Orlov, Ivan S.
Moiseeva, Anna A.
Butin, Kim P.
Sita, Lawrence R.
Egorov, Mikhail P.
Nefedov, Oleg M.
description The radical anion of di(2,6-diethylphenyl)stannylene (Ar 2Sn) has been generated by the electrochemical reduction of cyclotristannane cyclo-(Ar 2Sn) 3, and the electrochemical oxidation of cyclo-(Ar 2Sn) 3 resulted in Sn–Sn bond cleavage with the formation of the radical cation of tristannane.
doi_str_mv 10.1070/MC2002v012n04ABEH001601
format article
fullrecord <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1070_MC2002v012n04ABEH001601</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S095994360270624X</els_id><sourcerecordid>S095994360270624X</sourcerecordid><originalsourceid>FETCH-LOGICAL-c294t-d1144c99663eda04c08ad770d67cca4763f2e9522fd5dee879e7c45855ee7bf33</originalsourceid><addsrcrecordid>eNqFkE1OwzAQhb0AifJzBrIEqSljO4mbZakKRSpiU9aRsSfEyHUqO6rIzTgeTotQNwjNYqR5870ZPUKuKUwoCLh7njMAtgPKHGSz-8USgBZAT8gIyrxMy4wXZ-Q8hA8AEDmnI_K1sKg636oGNyZ0vk_aOqFjOmax-JinDX7KGzYuUm2wa3q7bdD19lb1yradj4h0TjqcJOsGk9r40CWR2GwthsEKj-yVtMk7OvSyM60bVJns-d7GaeKl3q9IN6jS6SgfXfjV1R6_JKe1tAGvfvoFeX1YrOfLdPXy-DSfrVLFyqxLNaVZpsqyKDhqCZmCqdRCgC6EUjITBa8Zljljtc414lSUKFSWT_McUbzVnF8QcfBVvg3BY11tvdlI31cUqiH06o_QIzk7kBjf2xn0VVAGnUJtfAyl0q351-MbAF6QOQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation</title><source>ScienceDirect Freedom Collection</source><creator>Orlov, Ivan S. ; Moiseeva, Anna A. ; Butin, Kim P. ; Sita, Lawrence R. ; Egorov, Mikhail P. ; Nefedov, Oleg M.</creator><creatorcontrib>Orlov, Ivan S. ; Moiseeva, Anna A. ; Butin, Kim P. ; Sita, Lawrence R. ; Egorov, Mikhail P. ; Nefedov, Oleg M.</creatorcontrib><description>The radical anion of di(2,6-diethylphenyl)stannylene (Ar 2Sn) has been generated by the electrochemical reduction of cyclotristannane cyclo-(Ar 2Sn) 3, and the electrochemical oxidation of cyclo-(Ar 2Sn) 3 resulted in Sn–Sn bond cleavage with the formation of the radical cation of tristannane.</description><identifier>ISSN: 0959-9436</identifier><identifier>DOI: 10.1070/MC2002v012n04ABEH001601</identifier><language>eng</language><publisher>Elsevier B.V</publisher><ispartof>Mendeleev communications, 2002, Vol.12 (4), p.125-126</ispartof><rights>2002 Russian Academy of Sciences</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c294t-d1144c99663eda04c08ad770d67cca4763f2e9522fd5dee879e7c45855ee7bf33</citedby><cites>FETCH-LOGICAL-c294t-d1144c99663eda04c08ad770d67cca4763f2e9522fd5dee879e7c45855ee7bf33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids></links><search><creatorcontrib>Orlov, Ivan S.</creatorcontrib><creatorcontrib>Moiseeva, Anna A.</creatorcontrib><creatorcontrib>Butin, Kim P.</creatorcontrib><creatorcontrib>Sita, Lawrence R.</creatorcontrib><creatorcontrib>Egorov, Mikhail P.</creatorcontrib><creatorcontrib>Nefedov, Oleg M.</creatorcontrib><title>Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation</title><title>Mendeleev communications</title><description>The radical anion of di(2,6-diethylphenyl)stannylene (Ar 2Sn) has been generated by the electrochemical reduction of cyclotristannane cyclo-(Ar 2Sn) 3, and the electrochemical oxidation of cyclo-(Ar 2Sn) 3 resulted in Sn–Sn bond cleavage with the formation of the radical cation of tristannane.</description><issn>0959-9436</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkE1OwzAQhb0AifJzBrIEqSljO4mbZakKRSpiU9aRsSfEyHUqO6rIzTgeTotQNwjNYqR5870ZPUKuKUwoCLh7njMAtgPKHGSz-8USgBZAT8gIyrxMy4wXZ-Q8hA8AEDmnI_K1sKg636oGNyZ0vk_aOqFjOmax-JinDX7KGzYuUm2wa3q7bdD19lb1yradj4h0TjqcJOsGk9r40CWR2GwthsEKj-yVtMk7OvSyM60bVJns-d7GaeKl3q9IN6jS6SgfXfjV1R6_JKe1tAGvfvoFeX1YrOfLdPXy-DSfrVLFyqxLNaVZpsqyKDhqCZmCqdRCgC6EUjITBa8Zljljtc414lSUKFSWT_McUbzVnF8QcfBVvg3BY11tvdlI31cUqiH06o_QIzk7kBjf2xn0VVAGnUJtfAyl0q351-MbAF6QOQ</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Orlov, Ivan S.</creator><creator>Moiseeva, Anna A.</creator><creator>Butin, Kim P.</creator><creator>Sita, Lawrence R.</creator><creator>Egorov, Mikhail P.</creator><creator>Nefedov, Oleg M.</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2002</creationdate><title>Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation</title><author>Orlov, Ivan S. ; Moiseeva, Anna A. ; Butin, Kim P. ; Sita, Lawrence R. ; Egorov, Mikhail P. ; Nefedov, Oleg M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c294t-d1144c99663eda04c08ad770d67cca4763f2e9522fd5dee879e7c45855ee7bf33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Orlov, Ivan S.</creatorcontrib><creatorcontrib>Moiseeva, Anna A.</creatorcontrib><creatorcontrib>Butin, Kim P.</creatorcontrib><creatorcontrib>Sita, Lawrence R.</creatorcontrib><creatorcontrib>Egorov, Mikhail P.</creatorcontrib><creatorcontrib>Nefedov, Oleg M.</creatorcontrib><collection>CrossRef</collection><jtitle>Mendeleev communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Orlov, Ivan S.</au><au>Moiseeva, Anna A.</au><au>Butin, Kim P.</au><au>Sita, Lawrence R.</au><au>Egorov, Mikhail P.</au><au>Nefedov, Oleg M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation</atitle><jtitle>Mendeleev communications</jtitle><date>2002</date><risdate>2002</risdate><volume>12</volume><issue>4</issue><spage>125</spage><epage>126</epage><pages>125-126</pages><issn>0959-9436</issn><abstract>The radical anion of di(2,6-diethylphenyl)stannylene (Ar 2Sn) has been generated by the electrochemical reduction of cyclotristannane cyclo-(Ar 2Sn) 3, and the electrochemical oxidation of cyclo-(Ar 2Sn) 3 resulted in Sn–Sn bond cleavage with the formation of the radical cation of tristannane.</abstract><pub>Elsevier B.V</pub><doi>10.1070/MC2002v012n04ABEH001601</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0959-9436
ispartof Mendeleev communications, 2002, Vol.12 (4), p.125-126
issn 0959-9436
language eng
recordid cdi_crossref_primary_10_1070_MC2002v012n04ABEH001601
source ScienceDirect Freedom Collection
title Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T21%3A46%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Electrochemistry%20of%201,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane.%20The%20first%20examples%20of%20electrochemical%20generation%20of%20a%20stannylene%20radical%20anion%20and%20a%20tristannane%20radical%20cation&rft.jtitle=Mendeleev%20communications&rft.au=Orlov,%20Ivan%20S.&rft.date=2002&rft.volume=12&rft.issue=4&rft.spage=125&rft.epage=126&rft.pages=125-126&rft.issn=0959-9436&rft_id=info:doi/10.1070/MC2002v012n04ABEH001601&rft_dat=%3Celsevier_cross%3ES095994360270624X%3C/elsevier_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c294t-d1144c99663eda04c08ad770d67cca4763f2e9522fd5dee879e7c45855ee7bf33%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