208
Y. Kubota
Liu Y, Niu L-Y, Liu X-L, Chen P-Z, Yao Y-S, Chen Y-Z, Yang Q-Z (2018) Synthesis of N, O,
B-chelated dipyrromethenes through an unexpected intramolecular cyclisation: enhanced nearinfrared emission in the aggregate/solid state. Chem Eur J 24:13549–13555
Liu K, Lalancette RA, Jäkle F (2019) Tuning the structure and electronic properties of B-N fused
dipyridylanthracene and implications on the self-sensitized reactivity with singlet oxygen. J Am
Chem Soc 141:7453–7462
Loudet A, Burgess K (2007) BODIPY dyes and their derivatives: syntheses and spectroscopic
properties. Chem Rev 107:4891–4932
Loudet A, Bandichhor R, Wu L, Burgess K (2008) Functionalized BF 2 chelated azadipyrromethene
dyes. Tetrahedron 64:3642–3654
Lower SK, El-Sayed MA (1966) The triplet state and molecular electronic processes in organic
molecules. Chem Rev 66:199–241
Lu H, Shimizu S, Mack J, Shen Z, Kobayashi N (2011) Synthesis and spectroscopic properties of
fused-ring-expanded aza-boradiazaindacenes. Chem Asian J 6:1026–1037
Lu H, Wang Q, Gai L, Li Z, Deng Y, Xiao X, Lai G, Shen Z (2012) Tuning the solid-state luminescence of BODIPY derivatives with bulky arylsilyl groups: synthesis and spectroscopic properties.
Chem Eur J 18:7852–7861
Lu H, Mack J, Yanga Y, Shen Z (2014) Structural modification strategies for the rational design of
red/NIR region BODIPYs. Chem Soc Rev 43:4778–4823
Lu H, Mack J, Nyokong T, Kobayashi N, Shen Z (2016) Optically active BODIPYs. Coord Chem
Rev 318:1–15
Lugovik KI, Eltyshev AK, Suntsova PO, Slepukhin PA, Benassi E, Belskaya NP (2018) Highlights
on the road towards highly emitting solid-state luminophores: two classes of thiazole-based
organoboron fluorophores with the AIEE/AIE effect. Chem Asian J 13:311–324
Lundrigan T, Thompson A (2013) Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the
reactivity of F-BODIPYs. J Org Chem 78:757–761
Lundrigan T, Baker AEG, Longobardi LE, Wood TE, Smithen DA, Crawford SM, Cameron TS,
Thompson A (2012a) An improved method for the synthesis of F-BODIPYs from dipyrrins and
bis(dipyrrin)s. Org Lett 14:2158–2161
Lundrigan T, Crawford SM, Cameron TS, Thompson A (2012b) Cl-BODIPYs: a BODIPY class
enabling facile B-substitution. Chem Commun 48:1003–1005
Lundrigan T, Cameron TS, Thompson A (2014) Activation and deprotection of F-BODIPYs using
boron trihalides. Chem Commun 50:7028–7031
Luo L, Wu D, Li W, Zhang S, Ma Y, Yan S, You J (2014) Regioselective decarboxylative direct C-H
arylation of boron dipyrromethenes (BODIPYs) at 2,6-positions: a facile access to a diversityoriented BODIPY library. Org Lett 16:6080–6083
Luo H-X, Niu Y, Jin X, Cao X-P, Yao X, Ye X-S (2016) Indolo-quinoline boron difluoride dyes:
synthesis and spectroscopic properties. Org Biomol Chem 14:4185–4188
Lv F, Yu Y, Hao E, Yu C, Wang H, Jiao L, Boens N (2018) Copper-catalyzed α-benzylation of
BODIPYs via radical-triggered oxidative cross-coupling of two C-H bonds. Chem Commun
54:9059–9062
Lv F, Tang B, Hao E, Liu Q, Wang H, Jiao L (2019) Transition-metal-free regioselective crosscoupling of BODIPYs with thiols. Chem Commun 55:1639–1642
Maar RR, Zhang R, Stephens DG, Ding Z, Gilroy JB (2019) Near-infrared photoluminescence and
electrochemiluminescence from a remarkably simple boron difluoride formazanate dye. Angew
Chem Int Ed 58:1052–1056
Macedo FP, Gwengo C, Lindeman SV, Smith MD, Gardinier JR (2008) β-diketonate, β-ketoiminate,
and β-diiminate complexes of difluoroboron. Eur J Inorg Chem 3200–3211
Maeda H, Haketa Y, Nakanishi T (2007) Aryl-substituted C 3 -bridged oligopyrroles as anion
receptors for formation of supramolecular organogels. J Am Chem Soc 129:13661–13674
Maeda C, Todaka T, Ueda T, Ema T (2016) Color-tunable solid-state fluorescence emission from
carbazole-based BODIPYs. Chem Eur J 22:7508–7513
Précédent

- 213/597

Suivant