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Articles

Simultaneous presence of mono- and bi-cationic bipyridyls within a metal-organic supramolecular host: crystal structure, spectral and Hirshfeld surface analysis

, , , ORCID Icon, ORCID Icon &
Pages 2742-2754 | Received 27 Mar 2022, Accepted 30 Oct 2022, Published online: 20 Dec 2022
 

Abstract

A new supramolecular metal-organic complex, {[Fe(CN)6]3-(H2bipy)2+(Hbipy)+·3H2O} (where bipy ipywhere biolecular metal-organic complex, {[Fe(CN)ccepted: 30 October 2022rized by single crystal X-ray crystallographic study (SC-XRD), powder X-ray diffraction (PXRD) and other spectroscopic analysis. Structural analysis reveals that the complex crystallizes in monoclinic space group P21/c and is a 3 D supramolecular complex. Cyanide-water hydrogen bonding interactions between {Fe(CN)6}3- and guest water molecules form a wave-like 2 D supramolecular layer structure parallel to the crystallographic ac-plane with the formation of rectangular cavities of dimension 10.6 × 9.8 Å. These 2 D layers are further connected by O3W-H2W3···O1W hydrogen bonding interactions to form a 3 D supramolecular structure with the creation of 1 D supramolecular channels along the crystallographic a-axis. The bi-cationic (H2bipy)2+ form two different N+-H···water hydrogen bonding interactions (N8+-H8···O2W and N7+-H7···O3W) with two different water molecules and reside within the rectangular cavities. Monocationic (Hbipy)+ moieties form a 1 D supramolecular chain structure through repetitive N···H-N+ hydrogen bonding interactions and are present within the 1 D supramolecular channels. In addition, these two different types of bipy moieties are interconnected to each other through π···π interactions. Hirshfeld surface analysis and the corresponding 2 D fingerprint plots clearly identify the presence of different types of supramolecular interactions between the two differently charged bipyridyl moieties and the host framework, and N-H/H-N contacts, corresponding to the hydrogen bonding interactions, have a significant contribution to the total surface. Both the absorption and emission spectra of the complex have also been studied.

Graphical Abstract

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This work was supported by funding from TARE, SERB to R.S. (TAR/2018/000744), and DST Inspire Faculty Research Grant to S.B. (DST/INSPIRE/04/2018/000329, Faculty Registration No.: IFA18-CH304). M.P. and S.K.D. thank DST Inspire Faculty Research Grant to S.B. for financial assistance. R.S. also acknowledges UGC for their STIDE GRANT to Kazi Nazrul University (Ref. No.: KNU/R/Letter/913/21).

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