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Synthesis and Characterization of New Cross-like Porphyrin-Naphthalocyanine and Porphyrin-Phthalocyanine Pentads
Synthesis and characterization of new cross‐like porphyrin–naphthalocyanine and porphyrin–phthalocyanine systems, where one naphthalocyanine and one phthalocyanine are the central moieties of the pentads, respectively, and in both cases substituted with four porphyrin units, in a cross‐shape structu...
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Published in: | Journal of heterocyclic chemistry 2014-08, Vol.51 (S1), p.E202-E208 |
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container_end_page | E208 |
container_issue | S1 |
container_start_page | E202 |
container_title | Journal of heterocyclic chemistry |
container_volume | 51 |
creator | Calvete, Mário J. F. Tomé, João P. C. Cavaleiro, José A. S. |
description | Synthesis and characterization of new cross‐like porphyrin–naphthalocyanine and porphyrin–phthalocyanine systems, where one naphthalocyanine and one phthalocyanine are the central moieties of the pentads, respectively, and in both cases substituted with four porphyrin units, in a cross‐shape structure. Porphyrin–naphthalonitrile and porphyrin–phthalonitrile adducts were prepared from the reaction of 5‐(p‐hydroxyphenyl)‐10,15,20‐triphenylporphyrin with the appropriate dihalogenated naphthalonitrile or phthalonitrile, respectively, to provide a straightforward cyclotetramerization in the presence of metallic magnesium, used as template. Spectroscopic characterization and initial photophysical assessment are also reported. |
doi_str_mv | 10.1002/jhet.1967 |
format | article |
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F. ; Tomé, João P. C. ; Cavaleiro, José A. S.</creator><creatorcontrib>Calvete, Mário J. F. ; Tomé, João P. C. ; Cavaleiro, José A. S.</creatorcontrib><description>Synthesis and characterization of new cross‐like porphyrin–naphthalocyanine and porphyrin–phthalocyanine systems, where one naphthalocyanine and one phthalocyanine are the central moieties of the pentads, respectively, and in both cases substituted with four porphyrin units, in a cross‐shape structure. Porphyrin–naphthalonitrile and porphyrin–phthalonitrile adducts were prepared from the reaction of 5‐(p‐hydroxyphenyl)‐10,15,20‐triphenylporphyrin with the appropriate dihalogenated naphthalonitrile or phthalonitrile, respectively, to provide a straightforward cyclotetramerization in the presence of metallic magnesium, used as template. 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Spectroscopic characterization and initial photophysical assessment are also reported.</description><subject>Adducts</subject><subject>Assessments</subject><subject>Magnesium</subject><subject>Porphyrins</subject><subject>Spectroscopic analysis</subject><subject>Spectroscopy</subject><subject>Synthesis</subject><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kNFO2zAUhi20SXQdF7xBJG7YRcDHjuP4ElVdC4JSiSK4s5zEUVxSJ7NTdeHpcSnatElcHVn_9x8dfwidAr4AjMnlutb9BYiUH6ERiITGDAT9gkYhIzEw8nyMvnm_Dk-gnI9Q9zDYvtbe-EjZMprUyqmi1868qt60NmqraKF30cS13seNedHRsnVdPThj44Xq6r5WTVsMyhqr3zf8jZf_hktte1X67-hrpRqvTz7mGD3-nK4m8_j2fnY9ubqNi4RmPE4hKTFAqQsmKMYcK8AFy0RKSsirkqR5wYALyrLwKcJSyPLQyCuRZLiiJKdjdH7Y27n211b7Xm6ML3TTKKvbrZeQEkETxtM0oGf_oet262y4TgJjnCeCB4lj9ONAFXsXTleyc2aj3CABy717uXcv9-4De3lgd6bRw-egvJlPVx-N-NAwvte__zSUe5Eh5Uw-LWYye55lZEXuZEbfAHDDlas</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Calvete, Mário J. 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S.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Calvete, Mário J. F.</au><au>Tomé, João P. C.</au><au>Cavaleiro, José A. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of New Cross-like Porphyrin-Naphthalocyanine and Porphyrin-Phthalocyanine Pentads</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><addtitle>J. Heterocyclic Chem</addtitle><date>2014-08</date><risdate>2014</risdate><volume>51</volume><issue>S1</issue><spage>E202</spage><epage>E208</epage><pages>E202-E208</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>Synthesis and characterization of new cross‐like porphyrin–naphthalocyanine and porphyrin–phthalocyanine systems, where one naphthalocyanine and one phthalocyanine are the central moieties of the pentads, respectively, and in both cases substituted with four porphyrin units, in a cross‐shape structure. Porphyrin–naphthalonitrile and porphyrin–phthalonitrile adducts were prepared from the reaction of 5‐(p‐hydroxyphenyl)‐10,15,20‐triphenylporphyrin with the appropriate dihalogenated naphthalonitrile or phthalonitrile, respectively, to provide a straightforward cyclotetramerization in the presence of metallic magnesium, used as template. 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identifier | ISSN: 0022-152X |
ispartof | Journal of heterocyclic chemistry, 2014-08, Vol.51 (S1), p.E202-E208 |
issn | 0022-152X 1943-5193 |
language | eng |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | Adducts Assessments Magnesium Porphyrins Spectroscopic analysis Spectroscopy Synthesis |
title | Synthesis and Characterization of New Cross-like Porphyrin-Naphthalocyanine and Porphyrin-Phthalocyanine Pentads |
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