It is difficult to
assemble multi-component metallo-supramolecular
architectures in a non-statistical fashion, which limits their development
toward functional materials. Herein, we report a system of interconverting
bowls and cages that are able to respond to various selective stimuli
(light, ligands, anions), based on the self-assembly of a photochromic
dithienylethene (DTE) ligand,
L
a
, with Pd
II
cations. By combining the concept of “coordination
sphere engineering”, relying on bulky quinoline donors, with
reversible photoswitching between the ligand’s open (
o
-
L
a
) and closed (
c
-
L
a
) forms, a [Pd
2
(
o
-
L
a
)
4
] cage (
o
-
C
) and a [Pd
2
(
c
-
L
a
)
3
] bowl (
c
-
B
) were obtained,
respectively. This structural rearrangement modulates the system’s
guest uptake capabilities. Among three bis-sulfonate guests (
G1
,
G2
, and
G3
), the cage can encapsulate
only the smallest (
G1
), while the bowl binds all of them.
Bowl
c
-
B
was further used to synthesize
a series of heteroleptic cages, [Pd
2
L
A
3
L
B
], representing a motif never reported before. Additional
ligands (
L
c-f
), with short
or long arms, tune the cavity size, thus enabling or preventing guest
uptake. Addition of Br
–
/Ag
+
makes it
possible to change the overall charge, again triggering guest uptake
and release, as well as fourth ligand de-/recomplexation. In combination,
site-selective introduction of functionality and application of external
stimuli lead to an intricate system of hosts with different guest
preferences. A high degree of complexity is achieved through cooperativity
between only a few components.