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Synthetic organic dyes are becoming the major class of water pollutants leading to malignant detriments to the ecology. Consequently, this research focuses on remediating this circumstance utilizing a novel catalytic material, namely, cerium-doped spinel ferrite Ni 0.6 Cu 0.4 Ce x Fe 2- x O 4 ( x = 0.0, 0.5, 1.0, 1.5), developed using the chemical coprecipitation technique and characterized using FTIR, XRD, FE-SEM, EDX and VSM analysis. The particles have shown band gap values ranging from 4.29 to 2.01 eV. The as-synthesized nano-sized particles were employed as a photocatalyst to degrade the complex structure of congo red (CR) dye. About 91% of the dye was degraded with 60 mg of the catalyst under visible light irradiation with the highest cerium-doping ( x = 1.5) at a pH below 6.8, which was the zero-surface charge pH for the particle. Batch studies were performed to optimize all the conditions, including the dose, concentration, pH, and different light energy sources. Recyclability of the catalyst was also investigated, which was supported by the higher stability of the recovered particles through XRD analysis. Reaction kinetics for this system were evaluated along with three isotherm models. Moreover, the scavenging test indicated that the major active species leading to this degradation was hole (h + ), and a schematic degradation mechanism is presented. Following that, this model can successfully be used for wastewater treatment., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (This journal is © The Royal Society of Chemistry.)

Triptycene derivatives are used extensively in supramolecular and materials chemistry, however, most are prepared using a multi-step synthesis involving the generation of a benzyne intermediate, which hinders production on a large scale. Inspired by the ease of the synthesis of resorcinarenes, we report the rapid and efficient preparation of triptycene-like 1,6,2',7'-tetrahydroxynaphthopleiadene directly from 2,7-dihydroxynaphthalene and phthalaldehyde. Structural characterisation confirms the novel bridged bicyclic framework, within which the planes of the single benzene ring and two naphthalene units are fixed at an angle of ∼120° relative to each other. Other combinations of aromatic 1,2-dialdehydes and 2,7-disubstituted naphthalenes also provided similar triptycene-like products. The low cost of the precursors and undemanding reaction conditions allow for rapid multigram synthesis of 1,6,2',7'-tetrahydroxynaphthopleiadene, which is shown to be a useful precursor for making the parent naphthopleiadene hydrocarbon. The great potential for the use of the naphthopleiadene scaffold in supramolecular and polymer chemistry is demonstrated by the preparation of a rigid novel cavitand, a microporous network polymer, and a solution-processable polymer of intrinsic microporosity., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)