212
Y. Kubota
Rao Y-L, Amarne H, Wang S (2012) Photochromic four-coordinate N, C-chelate boron compounds.
Coord Chem Rev 256:759–770
Rauschnabel J, Hanack M (1995) New derivatives and homologues of subphthalocyanine.
Tetrahedron Lett 36:1629–1632
Ray C, Díaz-Casado L, Avellanal-Zaballa E, Bañuelos J, Cerdán L, García-Moreno I, Moreno F,
Maroto BL, López-Arbeloa Í, de la Moya S (2017) N-BODIPYs come into play: smart dyes for
photonic materials. Chem Eur J 23:9383–9390
Ren Y, Liu X, Gao W, Xia H, Ye L, Mu Y (2007) Boron complexes with chelating anilido-imine
ligands: synthesis, structures and luminescent properties. Eur J Inorg Chem 1808–1814
Ren T-B, Xu W, Zhang W, Zhang X-X, Wang Z-Y, Xiang Z, Yuan L, Zhang X-B (2018) A general
method to increase Stokes shift by introducing alternating vibronic structures. J Am Chem Soc
140:7716–7722
Riddle JA, Lathrop SP, Bollinger JC, Lee D (2006) Schiff base route to stackable pseudotriphenylenes: stereoelectronic control of assembly and luminescence. J Am Chem Soc
128:10986–10987
Rodríuez-Morgade MS, Esperanza S, Torres T, Barberá J (2005) Synthesis, characterization, and
properties of subporphyrazines: a new class of nonplanar, aromatic macrocycles with absorption
in the green region. Chem Eur J 11:354–360
Rogers MAT (1943) 156. 2:4-diarylpyrroles. Part I. Synthesis of 2:4-diarylpyrroles and 2:2 :4:4 -
tetra-arylazadipyrromethines. J Chem Soc 590–596
Rohand T, Qin W, Boens N, Dehaen W (2006) Palladium-catalyzed coupling reactions for the
functionalization of BODIPY dyes with fluorescence spanning the visible spectrum. Eur J Org
Chem 4658–4663
Rohand T, Baruah M, Qin W, Boens N, Dehaen W (2006) Functionalisation of fluorescent BODIPY
dyes by nucleophilic substitution. Chem Commun 266–268
Roubinet B, Massif C, Moreau M, Boschetti F, Ulrich G, Ziessel R, Renard P-Y, Romieu A
(2015) New 3-(heteroaryl)-2-iminocoumarin-based borate complexes: synthesis, photophysical
properties, and rational functionalization for biosensing/biolabeling applications. Chem Eur J
21:14589–14601
Sakamoto N, Ikeda C, Nabeshima T (2010) Cation recognition and pseudorotaxane formation of
tris-dipyrrin BF 2 macrocycles. Chem Commun 46:6732–6734
Salla CAM, dos Santos JM, Farias G, Bortoluzi AJ, Curcio SF, Cazati T, Izsák R, Neese F, de Souza
B, Bechtold IH (2019) New boron(III) blue emitters for all-solution processed OLEDs: molecular
design assisted by theoretical modeling. Eur J Inorg Chem 2247–2257
Sarma T, Panda PK, Setsune J (2013) Bis-naphthobipyrrolylmethene derived BODIPY complex:
an intense near-infrared fluorescent dye. Chem Commun 49:9806–9808
Sathyamoorthi G, Soong M-L, Ross TW, Boyer JH (1993) Fluorescent tricyclic β-azavinamidine–
BF 2 complexes. Heteroat Chem 4:603–608
Sawazaki T, Shimizu Y, Oisaki K, Sohma Y, Kanai M (2018) Convergent and functional-grouptolerant synthesis of B-organo BODIPYs. Org Lett 20:7767–7770
Scheibe G, Daltrozzo E, Wörz O, Heiss J (1969) Das Franck-Condon-Prinzip und die Lichtabsorption von Merocyaninen. Z Phys Chem N F 64:97–114
Shaffer KJ, McLean TM, Waterland MR, Wenzel M, Plieger PG (2012) Structural characterisation
of difluoro-boron chelates of quino[7,8-h]quinoline. Inorg Chim Acta 380:278–283
Shah M, Thangaraj K, Soong ML, Wolford L, Boyer JH, Politzer I, Pavlopoulos TG (1990)
Pyrromethene–BF 2 complexes as laser dyes:1. Heteroat Chem 1:389–399
Shang H, Zhao L, Qi D, Chen C, Jiang J (2014) The first five-membered-heterocycle-fused subphthalocyanine analogues: chiral tri(benzo[b]thiopheno)subporphyrazines. Chem Eur J 20:16266–
16272
Shen Z, Röhr H, Rurack K, Uno H, Spieles M, Schulz B, Reck G, Ono N (2004) Borondiindomethene (BDI) dyes and their tetrahydrobicyclo precursors—en route to a new class of
highly emissive fluorophores for the red spectral range. Chem Eur J 10:4853–4871
Y. Kubota
Rao Y-L, Amarne H, Wang S (2012) Photochromic four-coordinate N, C-chelate boron compounds.
Coord Chem Rev 256:759–770
Rauschnabel J, Hanack M (1995) New derivatives and homologues of subphthalocyanine.
Tetrahedron Lett 36:1629–1632
Ray C, Díaz-Casado L, Avellanal-Zaballa E, Bañuelos J, Cerdán L, García-Moreno I, Moreno F,
Maroto BL, López-Arbeloa Í, de la Moya S (2017) N-BODIPYs come into play: smart dyes for
photonic materials. Chem Eur J 23:9383–9390
Ren Y, Liu X, Gao W, Xia H, Ye L, Mu Y (2007) Boron complexes with chelating anilido-imine
ligands: synthesis, structures and luminescent properties. Eur J Inorg Chem 1808–1814
Ren T-B, Xu W, Zhang W, Zhang X-X, Wang Z-Y, Xiang Z, Yuan L, Zhang X-B (2018) A general
method to increase Stokes shift by introducing alternating vibronic structures. J Am Chem Soc
140:7716–7722
Riddle JA, Lathrop SP, Bollinger JC, Lee D (2006) Schiff base route to stackable pseudotriphenylenes: stereoelectronic control of assembly and luminescence. J Am Chem Soc
128:10986–10987
Rodríuez-Morgade MS, Esperanza S, Torres T, Barberá J (2005) Synthesis, characterization, and
properties of subporphyrazines: a new class of nonplanar, aromatic macrocycles with absorption
in the green region. Chem Eur J 11:354–360
Rogers MAT (1943) 156. 2:4-diarylpyrroles. Part I. Synthesis of 2:4-diarylpyrroles and 2:2 :4:4 -
tetra-arylazadipyrromethines. J Chem Soc 590–596
Rohand T, Qin W, Boens N, Dehaen W (2006) Palladium-catalyzed coupling reactions for the
functionalization of BODIPY dyes with fluorescence spanning the visible spectrum. Eur J Org
Chem 4658–4663
Rohand T, Baruah M, Qin W, Boens N, Dehaen W (2006) Functionalisation of fluorescent BODIPY
dyes by nucleophilic substitution. Chem Commun 266–268
Roubinet B, Massif C, Moreau M, Boschetti F, Ulrich G, Ziessel R, Renard P-Y, Romieu A
(2015) New 3-(heteroaryl)-2-iminocoumarin-based borate complexes: synthesis, photophysical
properties, and rational functionalization for biosensing/biolabeling applications. Chem Eur J
21:14589–14601
Sakamoto N, Ikeda C, Nabeshima T (2010) Cation recognition and pseudorotaxane formation of
tris-dipyrrin BF 2 macrocycles. Chem Commun 46:6732–6734
Salla CAM, dos Santos JM, Farias G, Bortoluzi AJ, Curcio SF, Cazati T, Izsák R, Neese F, de Souza
B, Bechtold IH (2019) New boron(III) blue emitters for all-solution processed OLEDs: molecular
design assisted by theoretical modeling. Eur J Inorg Chem 2247–2257
Sarma T, Panda PK, Setsune J (2013) Bis-naphthobipyrrolylmethene derived BODIPY complex:
an intense near-infrared fluorescent dye. Chem Commun 49:9806–9808
Sathyamoorthi G, Soong M-L, Ross TW, Boyer JH (1993) Fluorescent tricyclic β-azavinamidine–
BF 2 complexes. Heteroat Chem 4:603–608
Sawazaki T, Shimizu Y, Oisaki K, Sohma Y, Kanai M (2018) Convergent and functional-grouptolerant synthesis of B-organo BODIPYs. Org Lett 20:7767–7770
Scheibe G, Daltrozzo E, Wörz O, Heiss J (1969) Das Franck-Condon-Prinzip und die Lichtabsorption von Merocyaninen. Z Phys Chem N F 64:97–114
Shaffer KJ, McLean TM, Waterland MR, Wenzel M, Plieger PG (2012) Structural characterisation
of difluoro-boron chelates of quino[7,8-h]quinoline. Inorg Chim Acta 380:278–283
Shah M, Thangaraj K, Soong ML, Wolford L, Boyer JH, Politzer I, Pavlopoulos TG (1990)
Pyrromethene–BF 2 complexes as laser dyes:1. Heteroat Chem 1:389–399
Shang H, Zhao L, Qi D, Chen C, Jiang J (2014) The first five-membered-heterocycle-fused subphthalocyanine analogues: chiral tri(benzo[b]thiopheno)subporphyrazines. Chem Eur J 20:16266–
16272
Shen Z, Röhr H, Rurack K, Uno H, Spieles M, Schulz B, Reck G, Ono N (2004) Borondiindomethene (BDI) dyes and their tetrahydrobicyclo precursors—en route to a new class of
highly emissive fluorophores for the red spectral range. Chem Eur J 10:4853–4871