340
K. Tanaka et al.
Tanaka K, Chujo Y (2012b) Advanced Luminescent Materials Based on Organoboron Polymers.
Macromol Rapid Commun 33(15):1235–1255
Tanaka K, Tamashima K, Nagai A, Okawa T, Chujo Y (2013) Facile modulation of optical properties
of diketonate-containing polymers by regulating complexation ratios with boron. Macromolecules
46(8):2969–2975
Tanaka K, Chujo Y (2013a) Chemicals-inspired biomaterials; developing biomaterials inspired by
material science based on POSS. Bull Chem Soc Jpn 86(11):1231–1239
Tanaka K, Kozuka H, Ueda K, Jeon J-H, Chujo Y (2017) POSS-based molecular fillers for simultaneously enhancing thermal and viscoelasticity of poly(methyl methacrylate) films. Mater Lett
203:62–67
Tang BZ et al (2015) Aggregation-induced emission: together we shine, united we soar! Chem Rev
115(21):11718–11940
Ueda K, Tanaka K, Chujo Y (2016) Remarkably high miscibility of octa-substituted poss with
commodity conjugated polymers and molecular fillers for the improvement of homogeneities of
polymer matrices. Polym J 48(12):1133–1139
Ueda K, Tanaka K, Chujo Y (2017) Synthesis of POSS derivatives having dual types of alkyl
substituents and their application as a molecular filler for low-refractive and highly durable
materials. Bull Chem Soc Jpn 90(2):205–209
Ueda K, Tanaka K, Chujo Y (2018) Fluoroalkyl POSS with dual functional groups as a molecular
filler for lowering refractive indices and improving thermomechanical properties of PMMA.
Polymers 10(12):1332
Ueda K, Tanaka K, Chujo Y (2019) Optical, electrical and thermal properties of organic−inorganic
hybrids with conjugated polymers based on poss having heterogeneous substituents. Polymers
11(1):44
Varughese S (2014) Non-covalent routes to tune the optical properties of molecular materials. J
Mater Chem C 2(18):3499–3516
Wakamiya A, Mori K, Yamaguchi S (2007) 3-Boryl-2,2’-bithiophene as a versatile core skeleton
for full-color highly emissive organic solids. Angew Chem Int Ed 46(23):4273–4276
Wang C et al (2015) Charge-transfer emission in organoboron-based biphenyls: effect of substitution
position and conformation. J Org Chem 80(21):10914–10924
Wang Y et al (2018) Twisted donor−acceptor cruciform luminophores possessing substituentdependent properties of aggregation-induced emission and mechanofluorochromism. J Phys
Chem C 122(4):2297–2306
Weber L et al (2012) Luminescence properties of c-diazaborolyl-ortho-carboranes as donor-acceptor
systems. Chem Eur J 18(27):8347–8357
Xu D et al (2018) Twisted donor–acceptor cruciform fluorophores exhibiting strong solid emission,
efficient aggregation-induced emission and high contrast mechanofluorochromism. Dyes Pigm
150:293–300
Xue S, Qiu X, Sun Q, Yang W (2016) Alkyl length effects on solid-state fluorescence and
mechanochromic behavior of small organic luminophores. J Mater Chem C 4(8):1568–1578
Yamaguchi M, Ito S, Hirose A, Tanaka K, Chujo Y (2017) Control of aggregation-induced emission
versus fluorescence aggregation-caused quenching by bond existence at a single site in boron
pyridinoiminate complexes. Mater Chem Front 1(8):1573–1579
Yamane H, Tanaka K, Chujo Y (2015) Simple and valid strategy for the enhancement of the solidemissive property based on boron dipyrromethene. Tetrahedron Lett 56(48):6786–6790
Yan W et al (2014) Synthesis, crystal structures and photophysical properties of novel boroncontaining derivatives of phenalene with bright solid-state luminescence. Dyes Pigm 106:197–
204
Yan H et al (2017) Design, synthesis and aggregation induced emission properties of two
bichromophores with a triphenylamine-coumarin dyad structure. Dyes Pigm 146:479–490
Yeo H, Tanaka K, Chujo Y (2013) Effective light-harvesting antennae based on bodipytethered cardo polyfluorenes via rapid energy transferring and low concentration quenching.
Macromolecules 46(7):2599–2605
K. Tanaka et al.
Tanaka K, Chujo Y (2012b) Advanced Luminescent Materials Based on Organoboron Polymers.
Macromol Rapid Commun 33(15):1235–1255
Tanaka K, Tamashima K, Nagai A, Okawa T, Chujo Y (2013) Facile modulation of optical properties
of diketonate-containing polymers by regulating complexation ratios with boron. Macromolecules
46(8):2969–2975
Tanaka K, Chujo Y (2013a) Chemicals-inspired biomaterials; developing biomaterials inspired by
material science based on POSS. Bull Chem Soc Jpn 86(11):1231–1239
Tanaka K, Kozuka H, Ueda K, Jeon J-H, Chujo Y (2017) POSS-based molecular fillers for simultaneously enhancing thermal and viscoelasticity of poly(methyl methacrylate) films. Mater Lett
203:62–67
Tang BZ et al (2015) Aggregation-induced emission: together we shine, united we soar! Chem Rev
115(21):11718–11940
Ueda K, Tanaka K, Chujo Y (2016) Remarkably high miscibility of octa-substituted poss with
commodity conjugated polymers and molecular fillers for the improvement of homogeneities of
polymer matrices. Polym J 48(12):1133–1139
Ueda K, Tanaka K, Chujo Y (2017) Synthesis of POSS derivatives having dual types of alkyl
substituents and their application as a molecular filler for low-refractive and highly durable
materials. Bull Chem Soc Jpn 90(2):205–209
Ueda K, Tanaka K, Chujo Y (2018) Fluoroalkyl POSS with dual functional groups as a molecular
filler for lowering refractive indices and improving thermomechanical properties of PMMA.
Polymers 10(12):1332
Ueda K, Tanaka K, Chujo Y (2019) Optical, electrical and thermal properties of organic−inorganic
hybrids with conjugated polymers based on poss having heterogeneous substituents. Polymers
11(1):44
Varughese S (2014) Non-covalent routes to tune the optical properties of molecular materials. J
Mater Chem C 2(18):3499–3516
Wakamiya A, Mori K, Yamaguchi S (2007) 3-Boryl-2,2’-bithiophene as a versatile core skeleton
for full-color highly emissive organic solids. Angew Chem Int Ed 46(23):4273–4276
Wang C et al (2015) Charge-transfer emission in organoboron-based biphenyls: effect of substitution
position and conformation. J Org Chem 80(21):10914–10924
Wang Y et al (2018) Twisted donor−acceptor cruciform luminophores possessing substituentdependent properties of aggregation-induced emission and mechanofluorochromism. J Phys
Chem C 122(4):2297–2306
Weber L et al (2012) Luminescence properties of c-diazaborolyl-ortho-carboranes as donor-acceptor
systems. Chem Eur J 18(27):8347–8357
Xu D et al (2018) Twisted donor–acceptor cruciform fluorophores exhibiting strong solid emission,
efficient aggregation-induced emission and high contrast mechanofluorochromism. Dyes Pigm
150:293–300
Xue S, Qiu X, Sun Q, Yang W (2016) Alkyl length effects on solid-state fluorescence and
mechanochromic behavior of small organic luminophores. J Mater Chem C 4(8):1568–1578
Yamaguchi M, Ito S, Hirose A, Tanaka K, Chujo Y (2017) Control of aggregation-induced emission
versus fluorescence aggregation-caused quenching by bond existence at a single site in boron
pyridinoiminate complexes. Mater Chem Front 1(8):1573–1579
Yamane H, Tanaka K, Chujo Y (2015) Simple and valid strategy for the enhancement of the solidemissive property based on boron dipyrromethene. Tetrahedron Lett 56(48):6786–6790
Yan W et al (2014) Synthesis, crystal structures and photophysical properties of novel boroncontaining derivatives of phenalene with bright solid-state luminescence. Dyes Pigm 106:197–
204
Yan H et al (2017) Design, synthesis and aggregation induced emission properties of two
bichromophores with a triphenylamine-coumarin dyad structure. Dyes Pigm 146:479–490
Yeo H, Tanaka K, Chujo Y (2013) Effective light-harvesting antennae based on bodipytethered cardo polyfluorenes via rapid energy transferring and low concentration quenching.
Macromolecules 46(7):2599–2605