Iodine-Rich Supramolecular Complexes of Chlorobismuthates(III): Unusual Lone Pair Activity and Features of Halogen Bonding in Crystals.

The first chrorobismuthate(III) supramolecular hybrids with halogen-bond-linked I2, (Py(CH2)2Py){[BiCl5](I2)} (1) and (Py(CH2)3Py){[BiCl5](I2)0.5} (2), were synthesized via the reaction between Bi2O3, I2, and salts of the corresponding cations in HCl. The compounds featured one- and two-dimensional (2D) supramolecular motifs built by I···Cl contacts; in the case of 1, Bi(III) is pentacoordinated due to the lone pair activity, which also interacted with I2 pi-orbitals, as confirmed by density functional theory (DFT) calculations. Both complexes exhibited moderate thermal stabilities and relatively narrow optical band gaps.

Discrete Hexa- and Binuclear Heterometallic Iodobismuthate(III) Complexes with Cu(I) and Ag(I).

The rare examples of discrete anionic halobismuthates(III) with group 11 elements were obtained. Those are (3-MePyH)6[Bi4Cu2I20] (1) and (3,5-MePyC6)3[BiAgI7]2 (2) (3-MePyH = 3-methylpyridinium cation, 3,5-MePyC6=1,6-bis(3,5-dimethylpyridinium)hexane dication). Both complexes were isolated as pure phases; the optical band gaps for 1 and 2 are 1.75 and 2.23 eV, respectively.

Copper and silver heterometallic iodoantimonates: structure, thermal stability, and optical properties.

Seven heterometallic iodoantimonates with the general formula (Cat)2{[Sb2M2I10]} (M = Cu(I) (1-6), Ag(I) (7)) were prepared. X-ray diffraction data indicate that these compounds are the first Sb(III) representatives of the structural type previously known only for heterometallic iodobismuthates(III). In 3 and 4, halogen-substituted cations form halogen bonds with the heterometallic halometalate chain. 1-7 show prominent thermal stability. The estimated optical band gaps lie between 2.16 and 2.40 eV. As in heterometallic iodobismuthates, incorporation of Cu+ rather than Ag+ provides a much lower band gap.

Copper- and Silver-Containing Heterometallic Iodobismuthates: Features of Thermochromic Behavior.

Nine heterometallic iodobismuthates with the general formula Cat2{[Bi2M2I10}] (M = Cu(I), Ag(I), Cat = organic cation) were synthesized. According to X-ray diffraction data, their crystal structures consisted of {Bi2I10} units interconnected with Cu(I) or Ag(I) atoms through I-bridging ligands, forming one-dimensional polymers. The compounds are thermally stable up to 200 °C. Optical band gaps (Eg), estimated at room temperature via diffuse reflectance measurements, range from 1.81 to 2.03 eV. Thermally induced changes in optical behavior (thermochromism) for compounds 1-9 were recorded, and general correlations were established. The thermal dependence of Eg appears to be close to linear for all studied compounds.

One-Dimensional Iodoantimonate(III) and Iodobismuthate(III) Supramolecular Hybrids with Diiodine: Structural Features, Stability and Optical Properties.

Two isostructural pairs of supramolecular iodoantimonate(III) and iodobismuthate(III) complexes with I2 units "trapped" in solid state via halogen bonding-Cat3[[M2I9](I2)} (Cat = tetramethylammonium and 1-methylpyridinium, M = Sb(III) and Bi(III)) were prepared. For all compounds, values of optical band gaps were determined, together with thermal stability; the complexes were additionally characterized by Raman spectroscopy.

Selenium(IV) Polybromide Complexes: Structural Diversity Driven by Halogen and Chalcogen Bonding.

Reactions between bromoselenate(IV)-containing solutions, dibromine and salts of pyridinium-family organic cations resulted in structurally diverse, bromine-rich polybromine-bromoselenates(IV): (4-MePyH)5[Se2Br9][SeBr6](Br3)2 (1), (2-MePyH)2{[SeBr6](Br2)} (2), (PyH)2{[SeBr5]Br(Br2)2} (3), (1-MePy)2{[SeBr6](Br2)} (4). The compounds feature halogen and (in the case of 3) chalcogen bonding in solid state, resulting in formation of supramolecular architectures of different dimensionality. DFT calculations allowed estimation of the energies of non-covalent interactions in 1-4; additionally, characterization by Raman spectroscopy was performed.

Supramolecular Diiodine-Bromostannate(IV) Complexes: Narrow Bandgap Semiconductors.

Three supramolecular bromostannates(IV) with "trapped" diiodine molecules, Cat2{[SnBr6](I2)} (Cat = Me4N+ (1), 1-MePy+ (2) and 4-MePyH (3)), were synthesized. In all cases, I2 linkers are connected with bromide ligands via halogen···halogen non-covalent interactions. Articles 1-3 were studied using Raman spectroscopy, thermogravimetric analysis, and diffuse reflectance spectroscopy. The latter indicates that 1-3 are narrow band gap semiconductors.

Oxochloroselenate(IV) with Incorporated {Cl2 }: The Case of Strong Cl⋠⋠⋠Cl Halogen Bonding.

Reaction of SeO2 , tetramethylammonium (TMA) chloride, aqueous HCl and Cl2 yields oxochloroselenate with incorporated Cl2 units, TMA3 {[Se2 O2 Cl7 ](Cl2 )}. The main feature of this compound is the strong (up to 3.5 kcal mol-1 , according to DFT calculations) Cl⋅⋅⋅Cl bonding, which is also detected by Raman spectroscopy.

Rule, Not Exclusion: Formation of Dichlorine-Containing Supramolecular Complexes with Chlorometalates(IV).

Supramolecular derivatives of chlorostannate(IV) and -plumbate(IV) with {Cl2} units, Cat2{[MCl6](Cl2)x} (1-5; M = Sn, Pb, cat = 1-methylpyridinium (1-MePy), tetramethylammonium (TMA)) were prepared and characterized by X-ray diffractometry and Raman spectroscopy. In particular, the TMA-containing complexes demonstrate remarkable thermal stability, releasing Cl2 only at elevated temperatures.

One-Dimensional Diiodine-Iodobismuthate(III) Hybrids Cat3{[Bi2I9](I2)3}: Syntheses, Stability, and Optical Properties.

One-dimensional iodine-rich iodobismuthates(III), Cat3{[Bi2I9](I2)3} [Cat = 1,4-MePy (1) and 1-EtBMAP (2)], feature the highest amount of "trapped" diiodine units in polyhalogen-halometalates of p-block elements. Both complexes have narrow optical band gaps (1.55 and 1.63 eV, respectively) and moderate thermal stability.