TY  - JOUR
AU  - Unniram Parambil, Ajmal Roshan
AU  - Pokratath, Rohan
AU  - Parammal, Muhammed Jibin
AU  - Dhaene, Evert
AU  - Van den Eynden, Dietger
AU  - Balog, Sandor
AU  - Prescimone, Alessandro
AU  - Infante, Ivan
AU  - Shahgaldian, Patrick
AU  - De Roo, Jonathan
TI  - Atomically precise surface chemistry of zirconium and hafnium metal oxo clusters beyond carboxylate ligands
JO  - Chemical science
VL  - 15
IS  - 42
SN  - 2041-6520
CY  - Cambridge
PB  - RSC
M1  - PUBDB-2025-00134
SP  - 17380-17396
PY  - 2024
AB  - The effectiveness of nanocrystals in many applications depends on their surface chemistry. Here, we leverage the atomically precise nature of zirconium and hafnium oxo clusters to gain fundamental insight into the thermodynamics of ligand binding. Through a combination of theoretical calculations and experimental spectroscopic techniques, we determine the interaction between the M6O88+ (M = Zr, Hf) cluster surface and various ligands: carboxylates, phosphonates, dialkylphosphinates, and monosubstituted phosphinates. We refute the common assumption that the adsorption energy of an adsorbate remains unaffected by the surrounding adsorbates. For example, dialkylphosphinic acids are too sterically hindered to yield complete ligand exchange, even though a single dialkylphosphinate has a high binding affinity. Monoalkyl or monoaryl phosphinic acids do replace carboxylates quantitatively and we obtained the crystal structure of M6O8H4(O2P(H)Ph)12 (M = Zr, Hf), giving insight into the binding mode of monosubstituted phosphinates. Phosphonic acids cause a partial structural reorganization of the metal oxo cluster into amorphous metal phosphonate as indicated by pair distribution function analysis. These results rationalize the absence of phosphonate-capped M6O8 clusters and the challenge in preparing Zr phosphonate metal–organic frameworks. We thus further reinforce the notion that monoalkylphosphinates are carboxylate mimics with superior binding affinity. 
LB  - PUB:(DE-HGF)16
C6  - pmid:39386907
UR  - <Go to ISI:>//WOS:001327118800001
DO  - DOI:10.1039/D4SC03859B
UR  - https://bib-pubdb1.desy.de/record/622022
ER  -