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• Main group compounds. • Inorganic-organic hybrid materials. • Nitrate inserted halobismuthates. • Mixed halobismuthates. Two binuclear halobismuthates (Bi 2 X 10)4− (X = Cl (1) and Br (2)) containing m -phenylenediammonium cation m PDA-(H) 2 2+ or m PDA-(H)]1+ starting from corresponding BiX 3 (X = Cl, Br) and their nitrate derivatives i.e., [Bi 2 X 8 (NO 3) 2 m PDA-(H) 2 2 (X = Cl (3) and Br (4)) starting from Bi(NO 3) 3 ,5H 2 O have been synthesized. 3 and 4 are the first examples of mixed halobismuthates where nitrate ions are coordinated to bismuth centers along with other halide ions. All the compounds have been characterized by single crystal XRD, elemental analysis and IR spectroscopy. The structural comparisons of 1 – 4 have been discussed. [ABSTRACT FROM AUTHOR]

Synthesis of iodobismuthates and tuning their properties attracted a lots of attention due to their contribution in developing opto-electronic devices. Two 1-D polymeric iodobismuthate compounds, {[2,6-(NH 2) 2 PyH][BiI 4 ]} n (1), {[4-NMe 2 PyH][BiI 4 ]} n (2), [Py: Pyridine] have been reported, where structurally similar polymeric anionic iodobismuthate is stabilised by two different pyridinium cations namely 2,6-bis(amino)pyridine and 4-(N , N -dimethylamino)pyridine derivatives. The compounds have been characterised by single crystal XRD, IR and elemental analysis. It is interesting to observe that the structurally similar compounds differ drastically in their optical properties because of slight variation in the cations. Comparison in structural features and their thermal, optical properties (band gap: 1.91 eV (1); 2.10 eV (2)) have been discussed. Thermochromism is exhibited by 1. DFT studies of compound 1 has been performed considering the crystal structure measured at two different temperature and the role of cation in tuning the optical properties of iodobismuthates has been established. [ABSTRACT FROM AUTHOR]