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   https://doi.org/10.1063/1.4963227  

   Korn, Joseph A. ; Tabor, Daniel P. ; Sibert, III, Edwin L. ; Zwier, Timothy S. ( September 2016 , The Journal of Chemical Physics)
2. Investigation of Bridgehead Effects on Reduction Potential in Alkyl and Aryl Azadithiolate-Bridged (µ-SCH 2 XCH 2 S) [Fe(CO) 3 ] 2 Synthetic Analogues of [FeFe]-H 2 ase Active Site: Investigation of Bridgehead Effects on Reduction Potential in Alkyl and Aryl Azadithiolate-Bridged (µ-SCH2XCH2S) [Fe(CO)3]2 Synthetic Analogues of [Fe

   https://doi.org/10.1002/ejic.201800335  

   Rana, Atanu ; Kumar Das, Pradip ; Mondal, Biswajit ; Dey, Subal ; Crouthers, Danielle ; Dey, Abhishek ( August 2018 , European Journal of Inorganic Chemistry)
3. Influence of Alkyl Chain Spacer Length on the Charge Carrier Mobility of Isotactic Poly( N -carbazolylalkyl acrylates)

   https://doi.org/10.1021/acsmacrolett.1c00249  

   Samal, Sanket ; Thompson, Barry C. ( June 2021 , ACS Macro Letters)

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4. Quantum state-resolved molecular scattering of NO (2Π1/2) at the gas-[C n mim][Tf 2 N] room temperature ionic liquid interface: Dependence on alkyl chain length, collision energy, and temperature

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   Zutz, Amelia ; Nesbitt, David J. ( October 2016 , AIP Advances)
5. Aqueous Self-Assembly of Peptide–Diketopyrrolopyrrole Conjugates with Variation of N-Alkyl Side Chain and π-Core Lengths

   https://doi.org/10.1055/a-1503-5912  

   Panda, Sayak Subhra ; Tovar, John D. ( April 2021 , Organic Materials)

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   Peptidic sequences when conjugated to π-electronic groups form self-assembled networks of π-electron pathways. These materials hold promise for bio-interfacing charge transporting applications because of their aqueous processability and compatibility. In this work, we incorporated diketopyrrolopyrrole (DPP), a well-established π-core for organic electronic applications, within the peptidic sequence. We embedded different numbers of thiophene rings (2 and 3) on both sides of the DPP to alter the length of the π-cores. We also varied the length of the N-alkyl side chains (methyl, butyl, hexyl) attached to the DPP core. These variations allowed us to explicitly study the effect of π-core and N-alkyl side-chain length on photophysical properties and morphology of the resulting nanomaterials. All of these molecules formed H-type aggregates in the assembled state. Longer π-cores have relatively red-shifted absorption maxima, whereas the N-alkyl variation did not present significant photophysical changes. 

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