RT info:eu-repo/semantics/article
T1 Uncovering the hidden landscape of Tris(4-pyridyl) ligands: Topological complexity derived from the bridgehead
A1 Waters, Jessica E.
A1 Berger, Georg
A1 Peel, Andrew J.
A1 García Rodríguez, Raúl
A1 Bond, Andrew D.
A1 Wright, Dominic Simon
K1 Coordination networks
K1 Redes de coordinación
K1 Pnictogens
K1 Pnictógeno
K1 Tripodal ligands
K1 Ligandos tripodales
K1 Topology
K1 Topología
AB Supramolecular main group chemistry is a developing field which parallels the conventional domain of metallo-organic chemistry. Little explored building blocks in this area are main group metal-based ligands which have the appropriate donor symmetry to build desired molecular or extended arrangements. Tris(pyridyl) main group ligands (E(py)3, E=main group metal) are potentially highly versatile building blocks since shifting the N-donor arms from the 2- to the 3-positions and 4-positions provides a very simple way of changing the ligand character from mononuclear/chelating to multidentate/metal-bridging. Here, the coordination behaviour of the first main group metal tris(4-pyridyl) ligands, E(4-py)3 (E=Sb, Bi, Ph−Sn) is explored, as well as their ability to build metal-organic frameworks (MOFs). The complicated topology of these MOFs shows a marked influence on the counter anion and on the ability of the E(4-py)3 ligands to switch coordination mode, depending on the steric and donor character of the bridgehead. This structure-directing influence of the bridgehead provides a potential building strategy for future molecular and MOF design in this area.
PB Wiley
SN 1521-3765
YR 2021
FD 2021
LK https://uvadoc.uva.es/handle/10324/49359
UL https://uvadoc.uva.es/handle/10324/49359
LA eng
NO Chemistry - A European Journal, 2021, vol. 27, n. 47. p. 12036-12040
NO Producción Científica
DS UVaDOC
RD 23-dic-2024