Four-Atom-Linked Capped Porphyrins: Synthesis and Characterization
Three new capped porphyrins, H2(OC2OPor) (7), H2(OC(CO)NPor) (13), and H2(OC2NPor) (14), to be used as heme model compounds, have been synthesized and characterized. These compounds have the shortest linkages between cap and porphyrin plane of any four-arm capped porphyrins synthesized to date. The...
Gespeichert in:
Veröffentlicht in: | Journal of organic chemistry 1996-05, Vol.61 (10), p.3298-3303 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3303 |
---|---|
container_issue | 10 |
container_start_page | 3298 |
container_title | Journal of organic chemistry |
container_volume | 61 |
creator | Johnson, Martin R Seok, Won K Ma, Wuping Slebodnick, Carla Wilcoxen, Keith M Ibers, James A |
description | Three new capped porphyrins, H2(OC2OPor) (7), H2(OC(CO)NPor) (13), and H2(OC2NPor) (14), to be used as heme model compounds, have been synthesized and characterized. These compounds have the shortest linkages between cap and porphyrin plane of any four-arm capped porphyrins synthesized to date. The general synthetic procedure for H2(OC2OPor) involves the reaction of a tetraaldehyde “cap” with pyrrole to form the capped porphyrin. In the synthesis of the tetraamide-capped porphyrin, H2(OC(CO)NPor), a tetraacid chloride cap is reacted with meso-α,α,α,α-tetra(o-aminophenyl)porphyrin. The amide groups may be reduced to form H2(OC2NPor). With the use of FeBr2, Fe2+ may be inserted in high yield into H2(OC2OPor) and H2(OC(CO)NPor). The crystal structures of H2(OC2NPor), Fe(OC2OPor)(OMe), and [Fe(OC2OPor)]2(μ-O) provide details on the types and amounts of cap expansion necessary to accommodate small ligands of biological interest, such as O2 and CO. |
doi_str_mv | 10.1021/jo9521615 |
format | Article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_jo9521615</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c677760892</sourcerecordid><originalsourceid>FETCH-LOGICAL-a295t-b51d1b7246e7b5a96c2c0bbd4553bd353238dc3011155de16cb8ecf8ec05aadc3</originalsourceid><addsrcrecordid>eNptj81KAzEUhYMoWKsL36AbFy6i-enNdNyV0lahYKHjOtxkUprWzgzJFKyrbn1Nn8RIpSsvXM7ifBz4CLnl7IEzwR_XdQ6CKw5npMNBMKpy1j8nHcaEoFIoeUmuYlyzdADQIeNJvQt02NZbOvPVxpW9ETZNinkdmtU--Co-fR--eot91a5c9LGHVWJWGNC2LvhPbH1dXZOLJb5Hd_OXXfI2GRejZzp7nb6MhjOKIoeWGuAlN5noK5cZwFxZYZkxZR9AmlKCFHJQWsk45wCl48qagbPL9AwQU9Ml98ddG-oYg1vqJvgthr3mTP_665N_YumR9bF1HycQw0arTGagi_lCi4FUOUxzXST-7sijjWlmF6pk8s_uD5v1aSg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Four-Atom-Linked Capped Porphyrins: Synthesis and Characterization</title><source>ACS Publications</source><creator>Johnson, Martin R ; Seok, Won K ; Ma, Wuping ; Slebodnick, Carla ; Wilcoxen, Keith M ; Ibers, James A</creator><creatorcontrib>Johnson, Martin R ; Seok, Won K ; Ma, Wuping ; Slebodnick, Carla ; Wilcoxen, Keith M ; Ibers, James A</creatorcontrib><description>Three new capped porphyrins, H2(OC2OPor) (7), H2(OC(CO)NPor) (13), and H2(OC2NPor) (14), to be used as heme model compounds, have been synthesized and characterized. These compounds have the shortest linkages between cap and porphyrin plane of any four-arm capped porphyrins synthesized to date. The general synthetic procedure for H2(OC2OPor) involves the reaction of a tetraaldehyde “cap” with pyrrole to form the capped porphyrin. In the synthesis of the tetraamide-capped porphyrin, H2(OC(CO)NPor), a tetraacid chloride cap is reacted with meso-α,α,α,α-tetra(o-aminophenyl)porphyrin. The amide groups may be reduced to form H2(OC2NPor). With the use of FeBr2, Fe2+ may be inserted in high yield into H2(OC2OPor) and H2(OC(CO)NPor). The crystal structures of H2(OC2NPor), Fe(OC2OPor)(OMe), and [Fe(OC2OPor)]2(μ-O) provide details on the types and amounts of cap expansion necessary to accommodate small ligands of biological interest, such as O2 and CO.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo9521615</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of organic chemistry, 1996-05, Vol.61 (10), p.3298-3303</ispartof><rights>Copyright © 1996 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a295t-b51d1b7246e7b5a96c2c0bbd4553bd353238dc3011155de16cb8ecf8ec05aadc3</citedby><cites>FETCH-LOGICAL-a295t-b51d1b7246e7b5a96c2c0bbd4553bd353238dc3011155de16cb8ecf8ec05aadc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jo9521615$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jo9521615$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>Johnson, Martin R</creatorcontrib><creatorcontrib>Seok, Won K</creatorcontrib><creatorcontrib>Ma, Wuping</creatorcontrib><creatorcontrib>Slebodnick, Carla</creatorcontrib><creatorcontrib>Wilcoxen, Keith M</creatorcontrib><creatorcontrib>Ibers, James A</creatorcontrib><title>Four-Atom-Linked Capped Porphyrins: Synthesis and Characterization</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>Three new capped porphyrins, H2(OC2OPor) (7), H2(OC(CO)NPor) (13), and H2(OC2NPor) (14), to be used as heme model compounds, have been synthesized and characterized. These compounds have the shortest linkages between cap and porphyrin plane of any four-arm capped porphyrins synthesized to date. The general synthetic procedure for H2(OC2OPor) involves the reaction of a tetraaldehyde “cap” with pyrrole to form the capped porphyrin. In the synthesis of the tetraamide-capped porphyrin, H2(OC(CO)NPor), a tetraacid chloride cap is reacted with meso-α,α,α,α-tetra(o-aminophenyl)porphyrin. The amide groups may be reduced to form H2(OC2NPor). With the use of FeBr2, Fe2+ may be inserted in high yield into H2(OC2OPor) and H2(OC(CO)NPor). The crystal structures of H2(OC2NPor), Fe(OC2OPor)(OMe), and [Fe(OC2OPor)]2(μ-O) provide details on the types and amounts of cap expansion necessary to accommodate small ligands of biological interest, such as O2 and CO.</description><issn>0022-3263</issn><issn>1520-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNptj81KAzEUhYMoWKsL36AbFy6i-enNdNyV0lahYKHjOtxkUprWzgzJFKyrbn1Nn8RIpSsvXM7ifBz4CLnl7IEzwR_XdQ6CKw5npMNBMKpy1j8nHcaEoFIoeUmuYlyzdADQIeNJvQt02NZbOvPVxpW9ETZNinkdmtU--Co-fR--eot91a5c9LGHVWJWGNC2LvhPbH1dXZOLJb5Hd_OXXfI2GRejZzp7nb6MhjOKIoeWGuAlN5noK5cZwFxZYZkxZR9AmlKCFHJQWsk45wCl48qagbPL9AwQU9Ml98ddG-oYg1vqJvgthr3mTP_665N_YumR9bF1HycQw0arTGagi_lCi4FUOUxzXST-7sijjWlmF6pk8s_uD5v1aSg</recordid><startdate>19960517</startdate><enddate>19960517</enddate><creator>Johnson, Martin R</creator><creator>Seok, Won K</creator><creator>Ma, Wuping</creator><creator>Slebodnick, Carla</creator><creator>Wilcoxen, Keith M</creator><creator>Ibers, James A</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19960517</creationdate><title>Four-Atom-Linked Capped Porphyrins: Synthesis and Characterization</title><author>Johnson, Martin R ; Seok, Won K ; Ma, Wuping ; Slebodnick, Carla ; Wilcoxen, Keith M ; Ibers, James A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a295t-b51d1b7246e7b5a96c2c0bbd4553bd353238dc3011155de16cb8ecf8ec05aadc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnson, Martin R</creatorcontrib><creatorcontrib>Seok, Won K</creatorcontrib><creatorcontrib>Ma, Wuping</creatorcontrib><creatorcontrib>Slebodnick, Carla</creatorcontrib><creatorcontrib>Wilcoxen, Keith M</creatorcontrib><creatorcontrib>Ibers, James A</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johnson, Martin R</au><au>Seok, Won K</au><au>Ma, Wuping</au><au>Slebodnick, Carla</au><au>Wilcoxen, Keith M</au><au>Ibers, James A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Four-Atom-Linked Capped Porphyrins: Synthesis and Characterization</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>1996-05-17</date><risdate>1996</risdate><volume>61</volume><issue>10</issue><spage>3298</spage><epage>3303</epage><pages>3298-3303</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><abstract>Three new capped porphyrins, H2(OC2OPor) (7), H2(OC(CO)NPor) (13), and H2(OC2NPor) (14), to be used as heme model compounds, have been synthesized and characterized. These compounds have the shortest linkages between cap and porphyrin plane of any four-arm capped porphyrins synthesized to date. The general synthetic procedure for H2(OC2OPor) involves the reaction of a tetraaldehyde “cap” with pyrrole to form the capped porphyrin. In the synthesis of the tetraamide-capped porphyrin, H2(OC(CO)NPor), a tetraacid chloride cap is reacted with meso-α,α,α,α-tetra(o-aminophenyl)porphyrin. The amide groups may be reduced to form H2(OC2NPor). With the use of FeBr2, Fe2+ may be inserted in high yield into H2(OC2OPor) and H2(OC(CO)NPor). The crystal structures of H2(OC2NPor), Fe(OC2OPor)(OMe), and [Fe(OC2OPor)]2(μ-O) provide details on the types and amounts of cap expansion necessary to accommodate small ligands of biological interest, such as O2 and CO.</abstract><pub>American Chemical Society</pub><doi>10.1021/jo9521615</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-3263 |
ispartof | Journal of organic chemistry, 1996-05, Vol.61 (10), p.3298-3303 |
issn | 0022-3263 1520-6904 |
language | eng |
recordid | cdi_crossref_primary_10_1021_jo9521615 |
source | ACS Publications |
title | Four-Atom-Linked Capped Porphyrins: Synthesis and Characterization |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T05%3A11%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Four-Atom-Linked%20Capped%20Porphyrins:%E2%80%89%20Synthesis%20and%20Characterization&rft.jtitle=Journal%20of%20organic%20chemistry&rft.au=Johnson,%20Martin%20R&rft.date=1996-05-17&rft.volume=61&rft.issue=10&rft.spage=3298&rft.epage=3303&rft.pages=3298-3303&rft.issn=0022-3263&rft.eissn=1520-6904&rft_id=info:doi/10.1021/jo9521615&rft_dat=%3Cacs_cross%3Ec677760892%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |