Extracurricular laboratory:new discovery of (Oxybis(2,1-phenylene))bis(diphenylphosphine)

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Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn¡¯t involve a screen. 166330-10-5, C36H28OP2. A document type is Article, introducing its new discovery., Application In Synthesis of (Oxybis(2,1-phenylene))bis(diphenylphosphine)

Two novel donor-pi-acceptor (D-pi-A type) porphyrin dyes were successfully synthesized and use in a dye-sensitized solar cell (DSSC). The molecular structures of both porphyrins are composed of the same dialkyl-substituted diphenylamino unit acting as the donor part, and two bisalkoxyphenyl substituents at the 5,15-meso positions. The acceptor part is composed of different ethyne-linked pi-extended bridges, and a cyanoacrylic acid (Dye I) or carboxyphenyl (Dye II) moiety acting as anchoring groups. In order to investigate the effects of including the pi-extended bridge between the porphyrin and acceptor unit, two different pi-extended bridges such as 2,2?-bithiophene and 2-(phenylethynyl)-thiophene, were employed. In particular, Dye II contains two triple bonds between donor substituted porphyrin and carboxylic acid group. These modifications could potentially reduce dye aggregation on the TiO2 surface. The charge recombination resistance and diffusion length for the cells with Dye II were relatively higher for all the measured ranges of bias potentials, implying that electron recombination loss from injected electrons was highly suppressed when Dye II molecules were adsorbed on the TiO2 surface. Eventually, Dye II containing a 2,2?-bithiophene pi-spacer and anchored trough a carboxyphenyl group exhibited a superior power conversion efficiency of 6.7% under AM 1.5 illumination (100 mW.cm-2) in a photoactive area of 0.46 cm 2 than Dye I with a 2-(phenylethynyl)thiophene (PCE = 3.5%) anchored through a cyanoacrylic group.

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Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate