1,7-Dipyrene-Containing Aza-BODIPYs: Are Pyrene Groups Effective as Ligands to Promote and Direct Complex Formation with Common Nanocarbon Materials?

Yuriy V. Zatsikha, Tanner S. Blesener, Philip C. Goff, Andrew T. Healy, Rachel K. Swedin, David E. Herbert, Gregory T. Rohde, Kullapa Chanawanno, Christopher J. Ziegler, Rodion V. Belosludov, David A. Blank, Victor N. Nemykin

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

A series of 1,7-dipyrene-aza-BODIPY and 1,7-dipyrene-3,5-diferrocene-aza-BODIPY derivatives 5a-e with pyrene ligands covalently attached to the β-pyrrolic positions of the boron-azadipyrromethene (aza-BODIPY) core have been prepared and characterized by NMR, UV-vis, and steady-state fluorescence spectroscopy; high-resolution mass spectrometry; and X-ray crystallography. The redox processes of these donor-acceptor aza-BODIPY systems were investigated by electrochemistry (cyclic voltammetry and differential pulse voltammetry methods) and spectroelectrochemistry. The potential of the closely spaced 1,7-dipyrene fragments to promote formation of noncovalent π-complexes with nanocarbon materials (C60, C70, (6,5)-single-walled carbon nanotube, and graphene) was explored. UV-vis, steady-state fluorescent, and time-resolved transient absorption spectroscopy data indicated that the interaction between the new pyrene-aza-BODIPYs and C60 or C70 fullerenes in solution is weak, and time-resolved transient absorption spectroscopy provided no evidence of photoinduced electron transfer. X-ray crystallography on a binary solid of aza-BODIPYs 5b and C60 was indicative of a pyrene-pyrene rather than pyrene-C60 interaction motif, whereas fullerenes were found to form close contacts with the electron-rich B,O-chelated part of aza-BODIPY 5b. In contrast, pyrene-pyrene and pyrene-C60 but not aza-BODIPY-C60 interactions were observed in the crystal structure of aza-BODIPY 5d and C60. Density functional theory (DFT) and time-dependent DFT calculations were used to support conclusions based on experimental data and are suggestive of rather weak interaction energies between 1,7-dipyrene-aza-BODIPYs and nanocarbon materials. Direct comparison with an analogous control compound lacking the pyrene ligands demonstrated that the pyrene substituents were ineffective at promoting and directing complex formation with nanocarbon materials. A common measurement of complex formation, emission loss in the presence of a nanocarbon acceptor, was demonstrated to have an alternative explanation in these systems, and the general effectiveness of using pyrene ligands to build noncovalent complexes was drawn into question.

Original languageEnglish (US)
Pages (from-to)27893-27916
Number of pages24
JournalJournal of Physical Chemistry C
Volume122
Issue number49
DOIs
StatePublished - Dec 13 2018

Bibliographical note

Funding Information:
Generous support from the Minnesota Supercomputing Institute, NSERC, CFI, NSF (CHE-1464711), NSF MRI (MRI-1420373 and MRI-0922366), University of Manitoba, and WestGrid Canada to V.N.N. is greatly appreciated. We also wish to thank Prof. Alex Nazarenko for help with the X-ray structure of 5b·C60. R.V.B. is grateful to the crew of Center for Computational Materials Science and E-IMR center at the Institute for Materials Research, Tohoku University, for continuous support and also thankful to the Ministry of Education, Culture, Sports, Science, and Technology of Japan (Grant No. 17H03122) for financial support. Generous support from the NSF support (DMR-1708177) to D.A.B. is greatly appreciated.

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