Open Access Article
Balázs
Szathmári
ab,
Tamás
Holczbauer
c,
Bence
Balterer
d,
Attila
Domján
d,
Balázs
Volk
e,
Ilona
Kovács
*a and
Zsolt
Kelemen
*ab
aDepartment of Inorganic and Analytical Chemistry, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3., H-1111 Budapest, Hungary. E-mail: kelemen.zsolt@vbk.bme.hu
bHUN-REN Computation Driven Chemistry Research Group, Budapest University of Technology and Economics, Műegyetem rkp. 3., H-1111 Budapest, Hungary
cChemical Crystallography Research Laboratory and Stereochemistry Research Group, Institute for Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar Tudósok krt. 2., H-1117 Budapest, Hungary
dNMR Research Laboratory, Centre for Structural Science, HUN-REN Research Centre for Natural Sciences, Magyar Tudósok krt. 2., H-1117 Budapest, Hungary
eDirectorate of Drug Substance Development, Egis Pharmaceuticals Plc, P.O. Box 100, H-1475 Budapest, Hungary
First published on 4th February 2026
Correction for ‘Synthesis and characterization of the first neutral hexacoordinated silole complexes’ by Balázs Szathmári et al., Chem. Commun., 2025, 61, 16042–16045, https://doi.org/10.1039/D5CC04234H.
The authors are grateful for the general support of János Bolyai Research Scholarship, OTKA (FK-145841) (ZK), DCEP, UCEP (EKÖP-24-3-BME-64) (BS) provided by the NKFIH). Part of the crystallographic study was carried out using the infrastructure of the Institute of Chemistry, Eötvös Loránd University (ELTE-CrystalLab), and the HUN-REN-ELTE Protein Modelling Research Group, and was supported by the European Union and the State of Hungary, and co-financed by the European Regional Development Fund (VEKOP-2.3.3-15-2017-00018).
The authors apologise for this omission.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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