Mono- and bis-Pd(II) complexes of N-confused dithiahexaphyrin(1.1.1.1.1.0) with the absorption and aromaticity modulated by Pd(II) coordination, macrocycle contraction and ancillary ligands

التفاصيل البيبلوغرافية
العنوان: Mono- and bis-Pd(II) complexes of N-confused dithiahexaphyrin(1.1.1.1.1.0) with the absorption and aromaticity modulated by Pd(II) coordination, macrocycle contraction and ancillary ligands
المؤلفون: Sun, Meng, Xie, Yongshu, Baryshnikov, Glib, Li, Chengjie, Sha, Feng, Wu, Xinyan, Ågren, Hans, Li, Shijun, Li, Qizhao
المصدر: Chemical Science. 15(6):2047-2054
الوصف: To further enrich the coordination chemistry of hexaphyrins and probe the underlying property–structural correlations, N-confused dithiahexaphyrin(1.1.1.1.1.0) (1) with 26 π-electron Hückel aromaticity was synthesized. Based on its unprecedented two unsymmetrical cavities, five palladium complexes 2, 3, 4-Ph, 4-Cl and 5 have been successfully synthesized under various coordinations. Thus, two mono-Pd(II) complexes 2 and 3 with the Pd(II) atom coordinated in the two different cavities were obtained by treating 1 with palladium reagents PdCl2, and (PPh3)2PdCl2 respectively. On this basis, bis-Pd(II) complexes 4-Ph and 4-Cl were synthesized by treating 2 and 3 with (PPh3)2PdCl2 and PdCl2, respectively. As a result, both 4-Ph and 4-Cl contain two Pd(II) atoms coordinated within the two cavities, with one of the Pd(II) atoms further coordinated to a triphenylphosphine ligand in addition to an anionic ancillary ligand of Ph− and Cl−, respectively. Notably, a further contracted mono-Pd(II) complex 5 was synthesized by treating 1 with Pd(PPh3)4 by eliminating one of the meso-carbon atoms together with the corresponding C6F5 moiety. These complexes present tunable 26 π aromaticity and NIR absorption up to 1060 nm. This work provides an effective approach for developing distinctive porphyrinoid Pd(II) complexes from a single porphyrinoid, without resorting to tedious syntheses of a series of porphyrinoid ligands.
وصف الملف: electronic
الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-531490Test
https://doi.org/10.1039/d3sc05473jTest
https://uu.diva-portal.org/smash/get/diva2:1872554/FULLTEXT01.pdfTest
قاعدة البيانات: SwePub