9 Molecular Designs for Solid-State Luminescent Properties …
341
Yeo H, Tanaka K, Chujo Y (2015b) Synthesis of dual-emissive polymers based on ineffective energy
transfer through cardo fluorene-containing conjugated polymers. Polymer 60:228–233
Yeo H, Tanaka K, Chujo Y (2015a) Energy transfer through heterogeneous dyes-substituted
fluorene-containing alternating copolymers and their dual-emission properties in the films. J
Polym Sci Part a: Polym Chem 53(17):2026–2035
Yoshii R, Nagai A, Tanaka K, Chujo Y (2014b) Boron ketoiminate-based polymers: fine-tuning of
the emission color and expression of strong emission both in the solution and film state. Macromol
Rapid Commun 35(15):1315–1319
Yoshii R, Suenaga K, Tanaka K, Chujo Y (2015) Mechanofluorochromic Materials Based on
Aggregation-Induced Emission-Active Boron Ketoiminates: Regulation of the Direction of the
Emission Color Changes. Chem Eur J 21(19):7231–7237
Yoshii R, Nagai A, Tanaka K, Chujo Y (2013) Highly emissive boron ketoiminate derivatives as
new class of aggregation-induced emission fluorophores. Chem Eur J 19(14):4506–4512
Yoshii R, Tanaka K, Chujo Y (2014a) Conjugated polymers based on tautomeric units: regulation
of main-chain conjugation and expression of aggregation induced emission property via boroncomplexation. Macromolecules 47(7):2268–2278
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014c) Boron diiminate with aggregation-induced emission
and crystallization-induced emission enhancement characteristics. Chem. Eur. J. 20(27):8320–
8324
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014d) Functionalization of boron diiminates with unique
optical properties: multicolor tuning of crystallization-induced emission and introduction into the
main-chain of conjugated polymers. J Am Chem Soc 136(52):18131–18139
Yu H-W, Kim B-S, Matsumoto S (2017) Effect of alkoxy side chain length on the solid-state
fluorescence behaviour of bisazomethine dyes possessing dipropylamino terminal group. Dyes
Pigm 136:131–139
Zhang M-Y et al (2018) Solid-state emissive triarylborane-based [2.2] paracyclophanes displaying
circularly polarized luminescence and thermally activated delayed fluorescence. Org Lett
20(15):6868−6871
Zhao C-H et al (2006) Highly emissive organic solids containing 2,5-diboryl-1,4-phenylene unit. J
Am Chem Soc 128(50):15934–15935
Zhao C-H, Wakamiya A, Yamaguchi S (2007) Highly emissive poly(aryleneethynylene)s containing
2,5-diboryl-1,4-phenylene as a building unit. Macromolecules 40(11):3898–3900
Zhu H et al (2018b) Twisted donor−π−acceptor carbazole luminophores with substituentdependent properties of aggregated behavior (aggregation-caused quenching to aggregationenhanced emission) and mechanoresponsive luminescence. J Phys Chem C 122(34):19793–19800
Zhu H et al (2018a) Branched triphenylamine luminophores: aggregation-induced fluorescence
emission, and tunable near-infrared solid-state fluorescence characteristics via external mechanical stimuli. Dyes Pigm 151:140–148
341
Yeo H, Tanaka K, Chujo Y (2015b) Synthesis of dual-emissive polymers based on ineffective energy
transfer through cardo fluorene-containing conjugated polymers. Polymer 60:228–233
Yeo H, Tanaka K, Chujo Y (2015a) Energy transfer through heterogeneous dyes-substituted
fluorene-containing alternating copolymers and their dual-emission properties in the films. J
Polym Sci Part a: Polym Chem 53(17):2026–2035
Yoshii R, Nagai A, Tanaka K, Chujo Y (2014b) Boron ketoiminate-based polymers: fine-tuning of
the emission color and expression of strong emission both in the solution and film state. Macromol
Rapid Commun 35(15):1315–1319
Yoshii R, Suenaga K, Tanaka K, Chujo Y (2015) Mechanofluorochromic Materials Based on
Aggregation-Induced Emission-Active Boron Ketoiminates: Regulation of the Direction of the
Emission Color Changes. Chem Eur J 21(19):7231–7237
Yoshii R, Nagai A, Tanaka K, Chujo Y (2013) Highly emissive boron ketoiminate derivatives as
new class of aggregation-induced emission fluorophores. Chem Eur J 19(14):4506–4512
Yoshii R, Tanaka K, Chujo Y (2014a) Conjugated polymers based on tautomeric units: regulation
of main-chain conjugation and expression of aggregation induced emission property via boroncomplexation. Macromolecules 47(7):2268–2278
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014c) Boron diiminate with aggregation-induced emission
and crystallization-induced emission enhancement characteristics. Chem. Eur. J. 20(27):8320–
8324
Yoshii R, Hirose A, Tanaka K, Chujo Y (2014d) Functionalization of boron diiminates with unique
optical properties: multicolor tuning of crystallization-induced emission and introduction into the
main-chain of conjugated polymers. J Am Chem Soc 136(52):18131–18139
Yu H-W, Kim B-S, Matsumoto S (2017) Effect of alkoxy side chain length on the solid-state
fluorescence behaviour of bisazomethine dyes possessing dipropylamino terminal group. Dyes
Pigm 136:131–139
Zhang M-Y et al (2018) Solid-state emissive triarylborane-based [2.2] paracyclophanes displaying
circularly polarized luminescence and thermally activated delayed fluorescence. Org Lett
20(15):6868−6871
Zhao C-H et al (2006) Highly emissive organic solids containing 2,5-diboryl-1,4-phenylene unit. J
Am Chem Soc 128(50):15934–15935
Zhao C-H, Wakamiya A, Yamaguchi S (2007) Highly emissive poly(aryleneethynylene)s containing
2,5-diboryl-1,4-phenylene as a building unit. Macromolecules 40(11):3898–3900
Zhu H et al (2018b) Twisted donor−π−acceptor carbazole luminophores with substituentdependent properties of aggregated behavior (aggregation-caused quenching to aggregationenhanced emission) and mechanoresponsive luminescence. J Phys Chem C 122(34):19793–19800
Zhu H et al (2018a) Branched triphenylamine luminophores: aggregation-induced fluorescence
emission, and tunable near-infrared solid-state fluorescence characteristics via external mechanical stimuli. Dyes Pigm 151:140–148