An update on the compound challenge: 1116-98-9

In some applications, this compound(1116-98-9)Application In Synthesis of tert-Butyl 2-cyanoacetate is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: tert-Butyl 2-cyanoacetate, is researched, Molecular C7H11NO2, CAS is 1116-98-9, about New semi-rigid triphenylamine donor moiety for D-π-A sensitizer: Theoretical and experimental investigations for DSSCs.Application In Synthesis of tert-Butyl 2-cyanoacetate.

Four novel dyes featuring new semi-rigid triphenylamine donor groups have been synthesized and successfully employed as sensitizers in dye-sensitized solar cells (DSSCs). Opting for the new semi-rigid triphenylamine (tPA) electron-donating unit yielded a better Voc and Jsc resulting to a power conversion efficiency (PCE) which is 16% higher compared to a reference dye whose electron-donating group is a conventional tPA unit. D. functional theory (DFT) and time-dependent DFT calculations revealed the more favorable charge-transport properties of the dye based on the new semi-rigid donor unit. Among the synthesized dyes, the DSSC device based on Dhkx-4 dye in conjunction with I-based electrolyte achieved a PCE of 6.23%, with Voc of 0.661 V, Jsc of 13.31 mA cm-2, and FF of 0.71 under simulated AM 1.5 G condition. Therefore, the novel semi-rigid tPA donor unit presented in this work is a promising donor group for a sensitizer in DSSCs and systematic structural engineering of the presented designs could offer valuable contributions for the development of the photovoltaic devices.

In some applications, this compound(1116-98-9)Application In Synthesis of tert-Butyl 2-cyanoacetate is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem