Selective one-step synthesis of triple-decker (porphyrinato)(phthalocyaninato) early lanthanides: the balance of concurrent processes

Kirill P Birin; Yulia G Gorbunova; Aslan Yu Tsivadze

doi:10.1039/c1dt11141h

Selective one-step synthesis of triple-decker (porphyrinato)(phthalocyaninato) early lanthanides: the balance of concurrent processes

Dalton Trans. 2011 Nov 21;40(43):11539-49. doi: 10.1039/c1dt11141h. Epub 2011 Sep 26.

Authors

Kirill P Birin¹, Yulia G Gorbunova, Aslan Yu Tsivadze

Affiliation

¹ A.N. Frumkin Institute of Physical Chemistry and Electrochemistry RAS, Leninsky pr., 31, 119991, Moscow, Russia.

PMID: 21952519
DOI: 10.1039/c1dt11141h

Abstract

An effective one-step approach for the preparation of (porphyrinato)(phthalocyaninato) early lanthanides of type [Br(4)TPP]Ln[(15C5)(4)Pc]Ln[Br(4)TPP], where Br(4)TPP = 5,10,15,20-tetrakis-(4-bromophenyl)-porphyrinato-ligand, (15C5)(4)Pc = tetrakis-(15-crown-5)-phthalocyaninato-ligand and Ln = La, Pr, Nd or Eu, is developed. The influence of various factors on the reaction pathway and yields of the complexes is investigated in detail. The developed protocol is found to be general for the early lanthanide subgroup. Variation of the synthetic conditions allowed the determination and isolation of possible side-products, namely heteroleptic double-deckers [Br(4)TPP]Ln[(15C5)(4)Pc] (Ln = Nd, Eu) and triple-decker [Br(4)TPP]Nd[(15C5)(4)Pc]Nd[(15C5)(4)Pc]. The peculiarities of the NMR lanthanide-induced shifts (LIS) of resonances of the synthesized triple-decker complexes are precisely investigated. The isostructurality of the synthesized complexes within the series as well as isostructurality with previously synthesized compounds is demonstrated in terms of two-nuclei analysis of LIS.