Loading…

Heterometallic Cu/Ln polymers active in the catalytic aerobic oxidation of cycloalkenes under solvent-free conditions

Heterometallic 3d-4f inorganic polymers were prepared using 3,5 pyridinedicarboxylic acid (H 2 PDC), {[CuLn 2 (PDC) 2 (SO 4 ) 2 (H 2 O) 6 ]·H 2 O} n (Ln: Sm III , CuSmPDC, Eu III , CuEuPDC, Gd III , and CuGdPDC). These catalysts are active in the aerobic oxidation of cycloalkenes under solvent-free...

Full description

Saved in:
Bibliographic Details
Published in:Dalton transactions : an international journal of inorganic chemistry 2018-10, Vol.47 (38), p.1336-13367
Main Authors: Cancino, P, Santibañez, L, Fuentealba, P, Olea, C, Vega, A, Spodine, E
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 13367
container_issue 38
container_start_page 1336
container_title Dalton transactions : an international journal of inorganic chemistry
container_volume 47
creator Cancino, P
Santibañez, L
Fuentealba, P
Olea, C
Vega, A
Spodine, E
description Heterometallic 3d-4f inorganic polymers were prepared using 3,5 pyridinedicarboxylic acid (H 2 PDC), {[CuLn 2 (PDC) 2 (SO 4 ) 2 (H 2 O) 6 ]·H 2 O} n (Ln: Sm III , CuSmPDC, Eu III , CuEuPDC, Gd III , and CuGdPDC). These catalysts are active in the aerobic oxidation of cycloalkenes under solvent-free conditions, with a conversion for the oxidation of cyclohexene of 71% after one hour of the reaction, and a TOF value of 1438 h −1 for CuSmPDC. On the other hand, the oxidation of cycloheptene and cyclooctene exhibited slightly lower conversions of 52% and 47%, and TOF values of 1053 and 159 h −1 after 1 and 6 hours of the reaction, respectively. The radical mechanism for the oxidation reaction of cyclohexene was assessed by Raman and EPR spectroscopy. The first evidenced the formation of Cu-O 2 adducts and the second permitted is to observe the presence of the oxygen centered radical species, which act as initiators of the reaction chain to generate the products. An increase in the temperature of the reaction correlates with the adduct formation, and with the enhancement of the oxidation reaction. Novel heterometallic 3d-4f inorganic polymers were studied as catalysts without an activator in solvent-free medium; the mechanism being demostrated by spectroscopy.
doi_str_mv 10.1039/c8dt01913d
format article
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c8dt01913d</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c8dt01913d</sourcerecordid><originalsourceid>FETCH-LOGICAL-r92t-19f8d16adb1c94a5e14f6f00d8aae73875dc836e52a081d29d0861a979bca7a83</originalsourceid><addsrcrecordid>eNpFkM1KAzEYRYMoWKsb90JeYGx-5idZyqBWKLjpvnyTfIPRNClJWpy3d0TR1b2Lc-7iEnLL2T1nUq-MsoVxzaU9Iwted12lhazP_7poL8lVzu-MCcEasSDHNRZMcY8FvHeG9sfVJtBD9NMeU6ZgijshdYGWN6QGZmoqMwazM8wZP52F4mKgcaRmMj6C_8CAmR6DxURz9CcMpRoTznoM1n3D-ZpcjOAz3vzmkmyfHrf9utq8Pr_0D5sqaVEqrkdleQt24EbX0CCvx3ZkzCoA7KTqGmuUbLERwBS3QlumWg6604OBDpRckruf2ZTN7pDcHtK0-79IfgHHVV1q</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Heterometallic Cu/Ln polymers active in the catalytic aerobic oxidation of cycloalkenes under solvent-free conditions</title><source>Royal Society of Chemistry</source><creator>Cancino, P ; Santibañez, L ; Fuentealba, P ; Olea, C ; Vega, A ; Spodine, E</creator><creatorcontrib>Cancino, P ; Santibañez, L ; Fuentealba, P ; Olea, C ; Vega, A ; Spodine, E</creatorcontrib><description>Heterometallic 3d-4f inorganic polymers were prepared using 3,5 pyridinedicarboxylic acid (H 2 PDC), {[CuLn 2 (PDC) 2 (SO 4 ) 2 (H 2 O) 6 ]·H 2 O} n (Ln: Sm III , CuSmPDC, Eu III , CuEuPDC, Gd III , and CuGdPDC). These catalysts are active in the aerobic oxidation of cycloalkenes under solvent-free conditions, with a conversion for the oxidation of cyclohexene of 71% after one hour of the reaction, and a TOF value of 1438 h −1 for CuSmPDC. On the other hand, the oxidation of cycloheptene and cyclooctene exhibited slightly lower conversions of 52% and 47%, and TOF values of 1053 and 159 h −1 after 1 and 6 hours of the reaction, respectively. The radical mechanism for the oxidation reaction of cyclohexene was assessed by Raman and EPR spectroscopy. The first evidenced the formation of Cu-O 2 adducts and the second permitted is to observe the presence of the oxygen centered radical species, which act as initiators of the reaction chain to generate the products. An increase in the temperature of the reaction correlates with the adduct formation, and with the enhancement of the oxidation reaction. Novel heterometallic 3d-4f inorganic polymers were studied as catalysts without an activator in solvent-free medium; the mechanism being demostrated by spectroscopy.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c8dt01913d</identifier><language>eng</language><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2018-10, Vol.47 (38), p.1336-13367</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>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Cancino, P</creatorcontrib><creatorcontrib>Santibañez, L</creatorcontrib><creatorcontrib>Fuentealba, P</creatorcontrib><creatorcontrib>Olea, C</creatorcontrib><creatorcontrib>Vega, A</creatorcontrib><creatorcontrib>Spodine, E</creatorcontrib><title>Heterometallic Cu/Ln polymers active in the catalytic aerobic oxidation of cycloalkenes under solvent-free conditions</title><title>Dalton transactions : an international journal of inorganic chemistry</title><description>Heterometallic 3d-4f inorganic polymers were prepared using 3,5 pyridinedicarboxylic acid (H 2 PDC), {[CuLn 2 (PDC) 2 (SO 4 ) 2 (H 2 O) 6 ]·H 2 O} n (Ln: Sm III , CuSmPDC, Eu III , CuEuPDC, Gd III , and CuGdPDC). These catalysts are active in the aerobic oxidation of cycloalkenes under solvent-free conditions, with a conversion for the oxidation of cyclohexene of 71% after one hour of the reaction, and a TOF value of 1438 h −1 for CuSmPDC. On the other hand, the oxidation of cycloheptene and cyclooctene exhibited slightly lower conversions of 52% and 47%, and TOF values of 1053 and 159 h −1 after 1 and 6 hours of the reaction, respectively. The radical mechanism for the oxidation reaction of cyclohexene was assessed by Raman and EPR spectroscopy. The first evidenced the formation of Cu-O 2 adducts and the second permitted is to observe the presence of the oxygen centered radical species, which act as initiators of the reaction chain to generate the products. An increase in the temperature of the reaction correlates with the adduct formation, and with the enhancement of the oxidation reaction. Novel heterometallic 3d-4f inorganic polymers were studied as catalysts without an activator in solvent-free medium; the mechanism being demostrated by spectroscopy.</description><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpFkM1KAzEYRYMoWKsb90JeYGx-5idZyqBWKLjpvnyTfIPRNClJWpy3d0TR1b2Lc-7iEnLL2T1nUq-MsoVxzaU9Iwted12lhazP_7poL8lVzu-MCcEasSDHNRZMcY8FvHeG9sfVJtBD9NMeU6ZgijshdYGWN6QGZmoqMwazM8wZP52F4mKgcaRmMj6C_8CAmR6DxURz9CcMpRoTznoM1n3D-ZpcjOAz3vzmkmyfHrf9utq8Pr_0D5sqaVEqrkdleQt24EbX0CCvx3ZkzCoA7KTqGmuUbLERwBS3QlumWg6604OBDpRckruf2ZTN7pDcHtK0-79IfgHHVV1q</recordid><startdate>20181002</startdate><enddate>20181002</enddate><creator>Cancino, P</creator><creator>Santibañez, L</creator><creator>Fuentealba, P</creator><creator>Olea, C</creator><creator>Vega, A</creator><creator>Spodine, E</creator><scope/></search><sort><creationdate>20181002</creationdate><title>Heterometallic Cu/Ln polymers active in the catalytic aerobic oxidation of cycloalkenes under solvent-free conditions</title><author>Cancino, P ; Santibañez, L ; Fuentealba, P ; Olea, C ; Vega, A ; Spodine, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-r92t-19f8d16adb1c94a5e14f6f00d8aae73875dc836e52a081d29d0861a979bca7a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cancino, P</creatorcontrib><creatorcontrib>Santibañez, L</creatorcontrib><creatorcontrib>Fuentealba, P</creatorcontrib><creatorcontrib>Olea, C</creatorcontrib><creatorcontrib>Vega, A</creatorcontrib><creatorcontrib>Spodine, E</creatorcontrib><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cancino, P</au><au>Santibañez, L</au><au>Fuentealba, P</au><au>Olea, C</au><au>Vega, A</au><au>Spodine, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterometallic Cu/Ln polymers active in the catalytic aerobic oxidation of cycloalkenes under solvent-free conditions</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><date>2018-10-02</date><risdate>2018</risdate><volume>47</volume><issue>38</issue><spage>1336</spage><epage>13367</epage><pages>1336-13367</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>Heterometallic 3d-4f inorganic polymers were prepared using 3,5 pyridinedicarboxylic acid (H 2 PDC), {[CuLn 2 (PDC) 2 (SO 4 ) 2 (H 2 O) 6 ]·H 2 O} n (Ln: Sm III , CuSmPDC, Eu III , CuEuPDC, Gd III , and CuGdPDC). These catalysts are active in the aerobic oxidation of cycloalkenes under solvent-free conditions, with a conversion for the oxidation of cyclohexene of 71% after one hour of the reaction, and a TOF value of 1438 h −1 for CuSmPDC. On the other hand, the oxidation of cycloheptene and cyclooctene exhibited slightly lower conversions of 52% and 47%, and TOF values of 1053 and 159 h −1 after 1 and 6 hours of the reaction, respectively. The radical mechanism for the oxidation reaction of cyclohexene was assessed by Raman and EPR spectroscopy. The first evidenced the formation of Cu-O 2 adducts and the second permitted is to observe the presence of the oxygen centered radical species, which act as initiators of the reaction chain to generate the products. An increase in the temperature of the reaction correlates with the adduct formation, and with the enhancement of the oxidation reaction. Novel heterometallic 3d-4f inorganic polymers were studied as catalysts without an activator in solvent-free medium; the mechanism being demostrated by spectroscopy.</abstract><doi>10.1039/c8dt01913d</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1477-9226
ispartof Dalton transactions : an international journal of inorganic chemistry, 2018-10, Vol.47 (38), p.1336-13367
issn 1477-9226
1477-9234
language eng
recordid cdi_rsc_primary_c8dt01913d
source Royal Society of Chemistry
title Heterometallic Cu/Ln polymers active in the catalytic aerobic oxidation of cycloalkenes under solvent-free conditions
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T01%3A19%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Heterometallic%20Cu/Ln%20polymers%20active%20in%20the%20catalytic%20aerobic%20oxidation%20of%20cycloalkenes%20under%20solvent-free%20conditions&rft.jtitle=Dalton%20transactions%20:%20an%20international%20journal%20of%20inorganic%20chemistry&rft.au=Cancino,%20P&rft.date=2018-10-02&rft.volume=47&rft.issue=38&rft.spage=1336&rft.epage=13367&rft.pages=1336-13367&rft.issn=1477-9226&rft.eissn=1477-9234&rft_id=info:doi/10.1039/c8dt01913d&rft_dat=%3Crsc%3Ec8dt01913d%3C/rsc%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-r92t-19f8d16adb1c94a5e14f6f00d8aae73875dc836e52a081d29d0861a979bca7a83%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