Two
series of OAc–-dependent unique homoleptic
nonanuclear [Ln9(L1)3(HL1)2(μ3-OH)4(OAc)10] (1–7) and hexanuclear
{[Ln6(L2)4(HL2)(μ3-OH)(OAc)2(H2O)2]·(OAc)} (8–14) are obtained
from the self-assembly of the partially deprotonated OH-H2Salen ligand H
3
L
1
(N,N′-bis(salicylidene)(propylene-2-ol)-1,3-diamine)
or OH-MeO-H2Salen ligand H
3
L
2
(N,N′-bis(3-methoxysalicylidene)(propylene-2-ol)-1,3-diamine)
with Ln(OAc)3 (Ln = La, Eu, Tb, Gd, Nd, Yb, or Er), respectively.
The result of their photophysical properties shows that the sensitization
for single-component near-white-light of complex 2, efficient
Eu3+-centered red-light (ΦL
Eu = 13.4%) of complex 9, or or Tb3+-centered
yellowish-green-light (ΦL
Tb = 8.1% and
21.3%) of complexes 3 and 10, and Nd3+- or Yb3+-centered NIR luminescence (η =
ΦL
Ln/ΦLn
Ln = 67–75% and 76–85%) for complexes 5–6 and 12–13, arose from the
ligands’ 3π–π* excited state,
due to effective intramolecular energy transfer and multiple Ln3+-to-Ln3+ electron-communications.