Chiroptical properties of 1,3-diphenylallene-anchored tetrathiafulvalene and its polymer synthesis

Scholarly Works

• Hasegawa, M.; Mazaki, Y. Stereogenic π-Conjugated Macrocycles: Synthesis, Structure, and Chiroptical Properties Including Circularly Polarized Luminescence. Synlett 2023. doi:10.1055/a-2158-8820
• Kahr, B.; Yang, Y.; Whittaker, S. J.; Shtukenberg, A. G.; Lee, S. Chiral Crystals, Jack, Conductivity and Magnetism. Helvetica Chimica Acta 2023, 106. doi:10.1002/hlca.202200202
• Galan, N. J.; Brantley, J. N. Precision Synthesis of Tunable Polyallenamers from "Masked" Precursors. Macromolecules 2022, 56, 305–310. doi:10.1021/acs.macromol.2c01968
• Yu, L.; Zhou, Q.; Gao, Y.; Fu, Z.; Xiao, Y.; Li, Z.-C.; Wang, J. Synthesis of polyallenoates through copper-mediated cross-coupling of dialkynes and bis-α-diazoesters. Chemical communications (Cambridge, England) 2022, 58, 3909–3912. doi:10.1039/d2cc00299j
• Topal, S.; Isci, R.; Topal, S.; Karakaya, O.; Amna, B.; Gunturkun, D.; Ozturk, T. Comprehensive Heterocyclic Chemistry IV - 1,3-Dithioles. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 834–994. doi:10.1016/b978-0-12-818655-8.00138-4
• Park, G.; Bielawski, C. W. Ring Opening Metathesis Polymerization of Cyclic Allenes. Macromolecules 2021, 54, 6135–6143. doi:10.1021/acs.macromol.1c00571
• Neary, W. J.; Sun, Y.; Moore, J. S. Selective Ring-Opening Allene Metathesis: Polymerization or Ruthenium Vinylidene Formation. ACS macro letters 2021, 10, 642–648. doi:10.1021/acsmacrolett.1c00229
• Galan, N. J.; Brantley, J. N. General Access to Allene-Containing Polymers Using the Skattebøl Rearrangement. ACS macro letters 2020, 9, 1662–1666. doi:10.1021/acsmacrolett.0c00745
• Garner, M. H.; Corminboeuf, C. Correlation between Optical Activity and the Helical Molecular Orbitals of Allene and Cumulenes. Organic letters 2020, 22, 8028–8033. doi:10.1021/acs.orglett.0c02980
• Yorimitsu, H.; Yoshimura, A.; Misaki, Y. Catalytic C–H Arylation of Tetrathiafulvalenes for the Synthesis of Functional Materials. Synthesis 2020, 52, 3326–3336. doi:10.1055/s-0040-1707256
• Hasegawa, M.; Iyoda, M. Self-Assembly of Radially π-Extended Tetrathiafulvalene Tetramers for Visible and Near Infrared Electrochromic Nanofiber. Bulletin of the Chemical Society of Japan 2019, 93, 154–162. doi:10.1246/bcsj.20190283
• Gaedke, M.; Witte, F.; Anhäuser, J.; Hupatz, H.; Schröder, H. V.; Valkonen, A.; Rissanen, K.; Lützen, A.; Paulus, B.; Schalley, C. A. Chiroptical inversion of a planar chiral redox-switchable rotaxane. Chemical science 2019, 10, 10003–10009. doi:10.1039/c9sc03694f
• Pop, F.; Zigon, N.; Avarvari, N. Main-Group-Based Electro- and Photoactive Chiral Materials. Chemical reviews 2019, 119, 8435–8478. doi:10.1021/acs.chemrev.8b00770
• Hasegawa, M.; Kurebayashi, D.; Matsuzawa, H.; Mazaki, Y. Chiroptical and Redox Properties of a Tetrathiafulvalene Analogue with an Inserted Spiro Framework. Chemistry Letters 2018, 47, 989–992. doi:10.1246/cl.180358
• Hasegawa, M.; Kobayakawa, K.; Matsuzawa, H.; Nishinaga, T.; Hirose, T.; Sako, K.; Mazaki, Y. Macrocyclic Oligothiophene with Stereogenic [2.2]Paracyclophane Scaffolds: Chiroptical Properties from π‐Transannular Interactions. Chemistry (Weinheim an der Bergstrasse, Germany) 2017, 23, 3267–3271. doi:10.1002/chem.201605842
• Aitken, R. A.; Dragomir, G.-I. Five-Membered Ring Systems. Progress in Heterocyclic Chemistry; Elsevier, 2016; pp 341–359. doi:10.1016/b978-0-08-100755-6.00010-7
• Hasegawa, M.; Iyoda, M. Organic Redox Systems - Tetrathiafulvalene: A Redox Unit for Functional Materials and a Building Block for Supramolecular Self-Assembly. Organic Redox Systems; Wiley, 2015; pp 89–129. doi:10.1002/9781118858981.ch4

Explore citations to this article at