Materials Science

9,9-Dimethyl-9,10-dihydroacridine.

9,9-Dimethyl-N,N-diphenyl-7-(4-(1-phenyl-1H-benzo[d ]imidazol-2-yl)phenyl)-9H-fluoren-2-amine.

9,9-Dimethyl-N,N-diphenyl-9H-fluoren-2-amine.

Application：This product offered here allows an ambient-air-tolerant method for negative electrode prelithiation prior to assembly of Li ion batteries. The redox potential of this product makes it useful for those most reported negative electrodes

Application：This product offered here allows an ambient-air-tolerant method for negative electrode prelithiation prior to assembly of Li ion batteries. The redox potential of this product makes it useful for those most reported negative electrodes

Application：This product offered here allows an ambient-air-tolerant method for negative electrode prelithiation prior to assembly of Li ion batteries. The redox potential of this product makes it useful for those most reported negative electrodes

Application：This product offered here allows an ambient-air-tolerant method for negative electrode prelithiation prior to assembly of Li ion batteries. The redox potential of this product makes it useful for those most reported negative electrodes

9,9-Dioctyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-9-silafluorene.

ApplicationThis material is used in the synthesis of low-band gap photovoltaic polymer materials that give power conversion efficiences of approx 3%.

9,9-Dioctyl-9H-fluoren-2-amine.

Application:It′s an aryl boronate ester. Arylboronic acids may be prepared by hydrolysis of boronate esters, and consequently many other boronic acid derivatives (e.g., organotrifluoroborates) are derived.

Application:It′s an aryl boronate ester. Arylboronic acids may be prepared by hydrolysis of boronate esters, and consequently many other boronic acid derivatives (e.g., organotrifluoroborates) are derived.