TY - JOUR
T1 - Supramolecular Singlet Fission of Pentacene Dimers within Polyaromatic Capsules
AU - Catti, Lorenzo
AU - Narita, Haruna
AU - Tanaka, Yuya
AU - Sakai, Hayato
AU - Hasobe, Taku
AU - Tkachenko, Nikolai V.
AU - Yoshizawa, Michito
N1 - Funding Information:
This work was supported by JSPS KAKENHI (Grant Nos. JP17H05359/ JP18H01990/ JP17K14476/ JP17H05381/ JP17H05270/ JP18H01957/ JP20KK0120, 20K05652, 20H05234, and JP21H01908) and “Support for Tokyotech Advanced Researchers (STAR)”. The computations were partly performed using Research Center for Computational Science, Okazaki, Japan. L.C. thanks the JSPS and Humboldt Postdoctoral Fellowship.
Publisher Copyright:
© 2021 American Chemical Society
PY - 2021/6/30
Y1 - 2021/6/30
N2 - We herein report a new set of supramolecular nanotools for the generation and modulation of singlet fission (SF) of noncovalent/covalent pentacene dimers. Two molecules of a pentacene monomer with bulky substituents are facilely encapsulated by a polyaromatic capsule, composed of naphthalene-based bent amphiphiles, in water. The encapsulated noncovalent dimer converts to otherwise undetectable triplet pairs and an individual triplet in high quantum yields (179% and 53%, respectively) even under high dilution conditions. Within the capsule, a covalently linked pentacene dimer with bulky groups generates two triplet pair intermediates in parallel, which are hardly distinguished in bulk solution, in excellent total quantum yield (196%). The yield of the individual triplet is enhanced by 1.6 times upon encapsulation. For both types of pentacene dimers, the SF features can be readily tuned by changing the polyaromatic panels of the capsule (i.e., anthracene and phenanthrene).
AB - We herein report a new set of supramolecular nanotools for the generation and modulation of singlet fission (SF) of noncovalent/covalent pentacene dimers. Two molecules of a pentacene monomer with bulky substituents are facilely encapsulated by a polyaromatic capsule, composed of naphthalene-based bent amphiphiles, in water. The encapsulated noncovalent dimer converts to otherwise undetectable triplet pairs and an individual triplet in high quantum yields (179% and 53%, respectively) even under high dilution conditions. Within the capsule, a covalently linked pentacene dimer with bulky groups generates two triplet pair intermediates in parallel, which are hardly distinguished in bulk solution, in excellent total quantum yield (196%). The yield of the individual triplet is enhanced by 1.6 times upon encapsulation. For both types of pentacene dimers, the SF features can be readily tuned by changing the polyaromatic panels of the capsule (i.e., anthracene and phenanthrene).
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U2 - 10.1021/jacs.0c13172
DO - 10.1021/jacs.0c13172
M3 - Article
C2 - 34133165
AN - SCOPUS:85110077083
SN - 0002-7863
VL - 143
SP - 9361
EP - 9367
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 25
ER -