TY - JOUR
T1 - Steric Control over Heteroleptic Trigonal Prisms
T2 - From Integrative Self-Sorting to Programmable Spin-State Modulation through Cage Transformations
AU - Chen, Yu Xiao
AU - Yue, Hua Liang
AU - Wu, Yu Qing
AU - Yu, Meng
AU - Tao, Jun
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2025/12/24
Y1 - 2025/12/24
N2 - The construction of well-defined heteroleptic assemblies via integrative self-sorting presents a persistent challenge in metal–organic cage (MOC) chemistry. Herein, we employ backbone steric constraints and precise edge-length complementarity to achieve a quantitative formation of heteroleptic trigonal-prismatic cages with the general formula [M6LA2L′3]12+ (M = Zn2+, Fe2+; L′ = LB, LC, and LD). The C3-symmetric tris-aniline ligand (LA) sterically directs a horizontal orientation of the three complementary rectangular ligands that thermodynamically disfavors the formation of competing homoleptic structures. The embedded tricoordinate sp2-boron centers render the Zn2+-based cage (1a-Zn) chemically addressable, enabling reversible fluoride binding to form a metastable adduct, which is quantitatively reversed through treatment with Ca2+ ions, demonstrating chemically gated cage-to-cage interconversion. Ligand exchange transforms a low-spin (LS) homoleptic cubic cage (4b-Fe, T1/2 = 371 K) into a heteroleptic trigonal-prismatic cage (2b-Fe, T1/2 = 272 K), resulting in an unusual ambient-temperature LS-to-HS spin transition. Furthermore, the structurally analogous imidazole-based cage (2a-Fe) exhibits permanent HS character, underscoring the tunability of spin states through subtle ligand modifications. To the best of our knowledge, 2b-Fe represents the first example of a SCO-active heteroleptic trigonal prism, thereby introducing a new structural archetype for hexanuclear Fe(II)-based SCO materials that extends beyond conventional coordination assemblies. These findings establish backbone steric bulk as a general approach to integrative self-sorting, demonstrate chemically triggered cage-to-cage transformations, and offer a versatile blueprint for encoding stimulus-responsive magnetism into discrete multinuclear cages.
AB - The construction of well-defined heteroleptic assemblies via integrative self-sorting presents a persistent challenge in metal–organic cage (MOC) chemistry. Herein, we employ backbone steric constraints and precise edge-length complementarity to achieve a quantitative formation of heteroleptic trigonal-prismatic cages with the general formula [M6LA2L′3]12+ (M = Zn2+, Fe2+; L′ = LB, LC, and LD). The C3-symmetric tris-aniline ligand (LA) sterically directs a horizontal orientation of the three complementary rectangular ligands that thermodynamically disfavors the formation of competing homoleptic structures. The embedded tricoordinate sp2-boron centers render the Zn2+-based cage (1a-Zn) chemically addressable, enabling reversible fluoride binding to form a metastable adduct, which is quantitatively reversed through treatment with Ca2+ ions, demonstrating chemically gated cage-to-cage interconversion. Ligand exchange transforms a low-spin (LS) homoleptic cubic cage (4b-Fe, T1/2 = 371 K) into a heteroleptic trigonal-prismatic cage (2b-Fe, T1/2 = 272 K), resulting in an unusual ambient-temperature LS-to-HS spin transition. Furthermore, the structurally analogous imidazole-based cage (2a-Fe) exhibits permanent HS character, underscoring the tunability of spin states through subtle ligand modifications. To the best of our knowledge, 2b-Fe represents the first example of a SCO-active heteroleptic trigonal prism, thereby introducing a new structural archetype for hexanuclear Fe(II)-based SCO materials that extends beyond conventional coordination assemblies. These findings establish backbone steric bulk as a general approach to integrative self-sorting, demonstrate chemically triggered cage-to-cage transformations, and offer a versatile blueprint for encoding stimulus-responsive magnetism into discrete multinuclear cages.
UR - https://www.scopus.com/pages/publications/105025686300
U2 - 10.1021/jacs.5c15226
DO - 10.1021/jacs.5c15226
M3 - Article
C2 - 41276971
AN - SCOPUS:105025686300
SN - 0002-7863
VL - 147
SP - 47311
EP - 47321
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 51
ER -