Compare the electrochemical and optical properties of the 1,7- and 1,6-regioisomers. Identify any differences in their performance that may result from their regioisomeric structure and diaryl substitution. Discuss the implications of these differences in the context of potential applications, such as in organic electronic devices or materials for sensors.
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1,7-bis(4-nitrophenyl)-N,N'-dioctyl-3:4,9:10-perylenetetracarboxydiimide
ethyl (2R,3S)-2-tert-butoxycarbonylamino-3-(4-(2-methoxyethoxymethoxy)phenyl)-3-methoxypropanoate
(2S)-(2,2-dichloroacetylamino)-(3R)-hydroxy-3-(4-nitrophenyl)-propionic acid ethyl ester
UCl3Li(THF)2(Me3SiNPPh2CPPh2NSiMe3)
N-[(4aR,6R,7R,8R,8aS)-6-[2-(2-Azido-ethoxy)-ethoxy]-8-(3-methoxy-benzyloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl]-acetamide
(1S,2S,3R)-1-(4-benzyloxy-3-methoxyphenyl)-3-[(S)-(4-benzyloxy-3-methoxyphenyl)(methoxymethoxy)methyl]-2-trityloxymethyl-1,4-butanediol
2,5-dimethoxybenzyl thioacetate
4H-Naphtho[2,3-e]-1,3-thiazin-4-one, 3-cyclohexyl-2-(cyclohexylimino)-2,3-dihydro-
anti-3-ethoxy-2-methyl-2-(phenylthio)cyclobutanone
1-acetoxy-3-chloro-1-phenyl-2-propanone
(S)-2-amino-3-methyl-N-phenylpentanamide
