| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1302036 | Inorganic Chemistry Communications | 2013 | 5 Pages |
1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) catalyzed esterification with 1-bromooctane over tetrakis/octakis(carboxy)phthalocyanines originated from trimellitic anhydride and pyromellitic dianhydride led to the isolation of a series of 2(3),9(10),16(17),24(25)-tetrakis(octyloxycarbonyl)phthalocyaninato metal complexes M[Pc(COOC8H17)4] (MCo, Ni, Cu, Zn) (1a–1d) and 2,3,9,10,16,17,24,25-octakis(octyloxycarbonyl)phthalocyaninato metal complexes M[Pc(COOC8H17)8] (MCo, Cu) (2a, 2c). In addition to elemental analysis, these tetrakis/octakis(octyloxycarbonyl)-substituted phthalocyanines were characterized by a series of spectroscopic methods including MALDI-TOF mass, 1H NMR and 2D COSY, UV–vis, and IR spectroscopy. The tetrakis(octyloxycarbonyl)-substituted phthalocyanines represent the first example of 2(3),9(10),16(17),24(25)-tetrakis(octyloxycarbonyl)phthalocyaninato metal complexes that have ever been unambiguously characterized by mass and NMR spectroscopy.
Graphical abstractTetrakis- and octakis-(octyloxycarbonyl)phthalocyaninato metal complexes isolated from trimellitic anhydride and pyromellitic dianhydride have been unambiguously characterized by a wide range of spectroscopic techniques, providing a reliable method for the synthesis of corresponding phthalocyanine compounds.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Phthalocyanines were synthesized from trimellitic anhydride/pyromellitic dianhydride. ► Synthesis octyloxycarbonyl substituted phthalocyanines by esterification reaction. ► Characterized by elemental analysis, MALDI-TOF mass, UV–vis, IR and NMR spectroscopy
