Making an inverted Keggin ion lacunary

Abstract

The century-old inverted Keggin ion has been revisited in an effort to unleash its potential in the structural engineering and functional development of polyoxomolybdates (POMos). Over the past hundred years, attempts to program the metal–oxo scaffold of inverted Keggins have been conducted continually but without any success. In this work, a structurally inert, inverted Keggin-type POMo could finally be altered by means of a binary heterogroup-templated approach, resulting in the successful isolation of two lacunary species. The local structure and charge distribution of these species are adjustable, and hence they serve as available building blocks for the subsequent controlled assembly of a Ce^III-incorporated derivative. From the plenary to the lacunary, the enclosed structure of the inverted Keggin has been opened up significantly, resulting in less steric hindrance, along with a transition from an electron neutral species to a negatively charged species. Owing to these beneficial properties, the emerging defect-containing polyanions demonstrated outstanding Lewis acid–base catalytic activity in the high efficiency production of pyrazoles.