Oxocyclohexadienylidene-Substituted Subporphyrins
Quinonoidal subporphyrin analogue 2 was synthesized by oxidation of meso‐tris(3,5‐di‐tert‐butyl‐4‐hydroxyphenyl)subporphyrin 1 (see scheme). Compound 2 was readily deprotonated to generate anionic species 3. These three macrocycles were structurally characterized, including the full delocalization o...
Saved in:
Published in | Angewandte Chemie International Edition Vol. 50; no. 14; pp. 3253 - 3256 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
28.03.2011
WILEY‐VCH Verlag Wiley Wiley Subscription Services, Inc |
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Quinonoidal subporphyrin analogue 2 was synthesized by oxidation of meso‐tris(3,5‐di‐tert‐butyl‐4‐hydroxyphenyl)subporphyrin 1 (see scheme). Compound 2 was readily deprotonated to generate anionic species 3. These three macrocycles were structurally characterized, including the full delocalization of the anionic charge in 3. |
---|---|
Bibliography: | MEXT - No. 22245006; No. 20108001 World Class University Program - No. R32-2008-000-10217-0 AFSOR/AOARD - No. FA 2386-09-1-4092 Ministry of Education and Human Resources Development, Korea ark:/67375/WNG-C21FSTW1-5 ArticleID:ANIE201006449 This work was supported by Grants-in-Aid (nos. 22245006 (A) and 20108001 "pi-Space") from MEXT. The work at Yonsei University was supported by World Class University Program (R32-2008-000-10217-0) and the Star Faculty program from the Ministry of Education and Human Resources Development, Korea, and AFSOR/AOARD grant (no. FA 2386-09-1-4092). istex:D67A090A0C5BBD10DB87DD402854C7CE349C16BE This work was supported by Grants‐in‐Aid (nos. 22245006 (A) and 20108001 “pi‐Space”) from MEXT. The work at Yonsei University was supported by World Class University Program (R32‐2008‐000‐10217‐0) and the Star Faculty program from the Ministry of Education and Human Resources Development, Korea, and AFSOR/AOARD grant (no. FA 2386‐09‐1‐4092). KAKEN ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201006449 |