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Handbook of Porphyrin Science, Vol. 1-10, Kadish KM, Smith KM and Guilard R. (Eds.) World Scientific: New Jersey, 2010.
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As pioneering examples: a) Aratani N, Osuka A, Kim YH, Jeong DH and Kim D. Angew. Chem., Int. Ed. 2000; 39: 1458-1462.
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Transition Metals in Supramolecular Chemistry, Sauvage JP. (Ed.) John Wiley & Sons: Chichester, 1999. b) Metal-Containing and Metallosupramolecular Polymers and Materials, Schubert US, Newkome GR and Manners I. (Eds.) ACS Symposium Series 928: Washington DC, 2006.
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As representative book and review article: , Springer- Verlag: Vienna,. b) Wood TE and Thompson A. Chem. Rev. 2007 c) Baudron SA CrystEngComm 2010 12: 2288-2295
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As representative book and review article: a) Falk H. The Chemistry of Linear Oligopyrroles and Bile Pigments, Springer-Verlag: Vienna, 1989. b) Wood TE and Thompson A. Chem. Rev. 2007; 107: 1831-1861. c) Baudron SA. CrystEngComm 2010; 12: 2288-2295.
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Nakanishi, T.6
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Meso-meso-linked BODIPY dimers: b) Whited MT Patel NM Roberts ST Allen K Djurovich PI Bradforth SE and Thompson ME Chem Commun 2012 48: 284-286
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Meso-meso-linked BODIPY dimers: a) Cakmak Y, Kolemen S, Duman S, Dede Y, Dolen Y, Kilic B, Kostereli Z, Yildirim LT, Dogan AL, Guc D and Akkaya EU. Angew. Chem., Int. Ed. 2011; 50: 11937-11941. b) Whited MT, Patel NM, Roberts ST, Allen K, Djurovich PI, Bradforth SE and Thompson ME. Chem. Commun. 2012; 48: 284-286.
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Dogan, A.L.9
Guc, D.10
Akkaya, E.U.11
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9
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57149091561
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Other directly linked BODIPY dimers: a) b) Bröring M, Kruger R, Link S, Kleeberg C, Kohler S, Xie X, Ventura B and Flamigni L. Chem. Eur. J. 2008 14 2976-2983 c) Ventura B Marconi G Bröring M Kruger R and Flamigni L New J Chem 2009 33 428-438 d) Rihn S Erdem M De Nicola A Retailleau P and Ziessel R Org Lett 2010 12 1916-1919 e) Hayashi Y Yamaguchi S Cha WY Kim D and Shinokubo H Org Lett 2010 12: 2992-2995
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Other directly linked BODIPY dimers: a) Bröring M, Bregier F, Kruger R and Kleeberg C. Eur. J. Inorg. Chem. 2008; 5505-5512. b) Bröring M, Kruger R, Link S, Kleeberg C, Kohler S, Xie X, Ventura B and Flamigni L. Chem. Eur. J. 2008; 14: 2976-2983. c) Ventura B, Marconi G, Bröring M, Kruger R and Flamigni L. New J. Chem. 2009; 33: 428-438. d) Rihn S, Erdem M, De Nicola A, Retailleau P and Ziessel R. Org. Lett. 2010; 12: 1916-1919. e) Hayashi Y. Yamaguchi S, Cha WY, Kim D and Shinokubo H. Org. Lett. 2010; 12: 2992-2995.
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Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Montgomery Jr., J.A.7
Vreven, T.8
Kudin, K.N.9
Burant, J.C.10
Millam, J.M.11
Iyengar, S.S.12
Tomasi, J.13
Barone, V.14
Mennucci, B.15
Cossi, M.16
Scalmani, G.17
Rega, N.18
Petersson, G.A.19
Nakatsuji, H.20
Hada, M.21
Ehara, M.22
Toyota, K.23
Fukuda, R.24
Hasegawa, J.25
Ishida, M.26
Nakajima, T.27
Honda, Y.28
Kitao, O.29
Nakai, H.30
Klene, M.31
Li, X.32
Knox, J.E.33
Hratchian, H.P.34
Cross, J.B.35
Adamo, C.36
Jaramillo, J.37
Gomperts, R.38
Stratmann, R.E.39
Yazyev, O.40
Austin, A.J.41
Cammi, R.42
Pomelli, C.43
Ochterski, J.W.44
Ayala, P.Y.45
Morokuma, K.46
Voth, G.A.47
Salvador, P.48
Dannenberg, J.J.49
Zakrzewski, V.G.50
Dapprich, S.51
Daniels, A.D.52
Strain, M.C.53
Farkas, O.54
Malick, D.K.55
Rabuck, A.D.56
Raghavachari, K.57
Foresman, J.B.58
Ortiz, J.V.59
Cui, Q.60
Baboul, A.G.61
Clifford, S.62
Cioslowski, J.63
Stefanov, B.B.64
Liu, G.65
Liashenko, A.66
Piskorz, P.67
Komaromi, I.68
Martin, R.L.69
Fox, D.J.70
Keith, T.71
Al-Laham, M.A.72
Peng, C.Y.73
Nanayakkara, A.74
Challacombe, M.75
Gill, P.M.W.76
Johnson, B.77
Chen, W.78
Wong, M.W.79
Gonzalez, C.80
Pople, J.A.81
more..
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14
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0000408854
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Similar Ring Closing Including An Oxidation Process Was Reported In Thienyl Derivative
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Similar ring closing including an oxidation process was reported in thienyl derivative: Fischer E, Larsen J, Christensen JB, Fourmigué M, Madsen HG and Harrit N. J. Org. Chem. 1996; 61: 6997-7005.
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Fischer, E.1
Larsen, J.2
Christensen, J.B.3
Fourmigué, M.4
Madsen, H.G.5
Harrit, N.6
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15
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84874123897
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C18H14N4, Mw = 286.33, monoclinic, P21/a. no 14) a =9.720 (2), b = 18.990(5), c = 15.098(5) Å, β =99.347(10)°, V = 2749.9(12) Å3, Z = 8, Dc = 1.383 g cm-3, T = 123 2) K, μ(Mo-Kα) = 0.086 mm-1, R1= 0.0433, wR2 = 0.1033, GOF = 1.025 (I > 2σ (I)). CCDC 875752
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Crystal data for 3 (from CH2Cl2/hexane): C18H14N4, Mw = 286.33, monoclinic, P21/a (no. 14), a =9.720(2), b = 18.990(5), c = 15.098(5) Å, β =99.347(10)°, V = 2749.9(12) Å3, Z = 8, Dc = 1.383 g cm-3, T = 123(2) K, μ(Mo-Kα) = 0.086 mm-1, R1= 0.0433, wR2 = 0.1033, GOF = 1.025 (I > 2σ (I)). CCDC 875752.
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Crystal data for 3 (from CH2Cl2/hexane)
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