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Volumn 10, Issue 27, 2008, Pages 3982-3986

Photoinduced intercomponent processes in multichromophoric species made of Pt(II)-terpyridine-acetylide and dipyrromethene-BF2 subunits

(5) Nastasi, Francesco a Puntoriero, Fausto a Campagna, Sebastiano a Diring, Stéphane b Ziessel, Raymond b

a UNIVERSITY OF MESSINA (Italy)

b UNIVERSITÉ DE STRASBOURG (France)

Author keywords

[No Author keywords available]

Indexed keywords

DIPYRROMETHENE; DRUG DERIVATIVE; FLUORESCENT DYE; PLATINUM COMPLEX; PORPHOBILINOGEN; PYRIDINIUM DERIVATIVE; RUTHENIUM;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; ENERGY TRANSFER; LUMINESCENCE; OXIDATION REDUCTION REACTION; PHOTOCHEMISTRY; SYNTHESIS; ULTRAVIOLET RADIATION;

ENERGY TRANSFER; FLUORESCENT DYES; LUMINESCENCE; MOLECULAR STRUCTURE; ORGANOPLATINUM COMPOUNDS; OXIDATION-REDUCTION; PHOTOCHEMISTRY; PORPHOBILINOGEN; PYRIDINIUM COMPOUNDS; RUTHENIUM; ULTRAVIOLET RAYS;

EID: 46449104781 PISSN: 14639076 EISSN: None Source Type: Journal
DOI: 10.1039/b805972a Document Type: Article

Times cited : (62)

References (22)

1
- 0012317549
- Wiley-VCH, Weinheim, This topic is too vast to be exhaustively cited. For recent reviews, see the following:
- V. Balzani, A. Credi and M. Venturi, Molecular Devices and Machines, Wiley-VCH, Weinheim, 2003, ch. 2-6 and references therein
- (2003) Molecular Devices and Machines
- Balzani, V.¹ Credi, A.² Venturi, M.³

2
- 0000891174
- A. Harriman R. Ziessel Coord. Chem. Rev. 1998 171 331
- (1998) Coord. Chem. Rev. , vol.171 , pp. 331
- Harriman, A.¹ Ziessel, R.²

3
- 0002524543
- V. Balzani S. Campagna G. Denti A. Juris S. Serroni M. Venturi Acc. Chem. Res. 1998 31 26
- (1998) Acc. Chem. Res. , vol.31 , pp. 26
- Balzani, V.¹ Campagna, S.² Denti, G.³ Juris, A.⁴ Serroni, S.⁵ Venturi, M.⁶

4
- 0034391542
- F. Barigelletti L. Flamigni Chem. Soc. Rev. 2000 29 1
- (2000) Chem. Soc. Rev. , vol.29 , pp. 1
- Barigelletti, F.¹ Flamigni, L.²

5
- 2342649581
- E. Baranoff J.-P. Collin L. Flamigni J.-P. Sauvage Chem. Soc. Rev. 2004 33 147
- (2004) Chem. Soc. Rev. , vol.33 , pp. 147
- Baranoff, E.¹ Collin, J.-P.² Flamigni, L.³ Sauvage, J.-P.⁴

6
- 26944498967
- J. H. Alstrum-Acevedo M. K. Brennaman T. J. Meyer Inorg. Chem. 2005 44 6802
- (2005) Inorg. Chem. , vol.44 , pp. 6802
- Alstrum-Acevedo, J.H.¹ Brennaman, M.K.² Meyer, T.J.³

7
- 33847233658
- S. Rau D. Walther J. G. Vos Dalton Trans. 2007 915
- (2007) Dalton Trans. , pp. 915
- Rau, S.¹ Walther, D.² Vos, J.G.³

8
- 25144445265
- M. Galletta S. Campagna M. Quesada G. Ulrich R. Ziessel Chem. Commun. 2005 4222
- (2005) Chem. Commun. , pp. 4222
- Galletta, M.¹ Campagna, S.² Quesada, M.³ Ulrich, G.⁴ Ziessel, R.⁵

9
- 33646402920
- For recent multichromophores containing Pt(ii) polypyridine subunits, see:
- M. Galletta F. Puntoriero S. Campagna C. Chiorboli M. Quesada S. Goeb R. Ziessel J. Phys. Chem. A 2006 110 4348
- (2006) J. Phys. Chem. a , vol.110 , pp. 4348
- Galletta, M.¹ Puntoriero, F.² Campagna, S.³ Chiorboli, C.⁴ Quesada, M.⁵ Goeb, S.⁶ Ziessel, R.⁷

10
- 26944442709
- S. Chakravorthy T. J. Wadas H. Hester S. Schmehl R. Eisenberg Inorg. Chem. 2005 44 6865
- (2005) Inorg. Chem. , vol.44 , pp. 6865
- Chakravorthy, S.¹ Wadas, T.J.² Hester, H.³ Schmehl, S.⁴ Eisenberg, R.⁵

11
- 34547840324
- J. A. G. Williams Top. Curr. Chem. 2007 281 205
- (2007) Top. Curr. Chem. , vol.281 , pp. 205
- Williams, J.A.G.¹

12
- 40849137742
- R. Ziessel J. B. Seneclauze B. Ventura A. Barbieri F. Barigelletti Dalton Trans. 2008 1686
- (2008) Dalton Trans. , pp. 1686
- Ziessel, R.¹ Seneclauze, J.B.² Ventura, B.³ Barbieri, A.⁴ Barigelletti, F.⁵

13
- 1642308744
- G. Ulrich R. Ziessel J. Org. Chem. 2004 69 2070
- (2004) J. Org. Chem. , vol.69 , pp. 2070
- Ulrich, G.¹ Ziessel, R.²

14
- 0035969301
- V. W.-W. Yam R. P.-L. Tang K. M.-C. Wong K.-K. Cheung Organometallics 2001 20 4476
- (2001) Organometallics , vol.20 , pp. 4476
- Yam, V.W.-W.¹ Tang, R.P.-L.² Wong, K.M.-C.³ Cheung, K.-K.⁴

15
- 0011633872
- M. Howe-Grant S. J. Lippard Inorg. Synth. 1980 20 102
- (1980) Inorg. Synth. , vol.20 , pp. 102
- Howe-Grant, M.¹ Lippard, S.J.²

16
- 33645769193
- Because of the different percentage of the bodipy luminescence quantum yield reduction and lifetime shortening on passing from model species to 4 at room temperature, such effects cannot be safely attributed to an intercomponent quenching process. Increased spin-orbit coupling induced by the presence of the heavy metal could also accelerate intersystem crossing within the bodipy dye. On these bases, at a first approximation here we consider intercomponent quenching processes ineffective for the decay of the bodipy singlet state, also at room temperature There are several reports of charge-separated states which collapse to lower-lying triplet states in multichromophoric species. See ref. 3 and the following recent papers:
- R. Ziessel L. Bonardi P. Retailleau G. Ulrich J. Org. Chem. 2006 71 3093
- (2006) J. Org. Chem. , vol.71 , pp. 3093
- Ziessel, R.¹ Bonardi, L.² Retailleau, P.³ Ulrich, G.⁴

17
- 28044466668
- A. C. Benniston A. Harriman P. Li J. P. Rostron H. J. van Ramesdonk M. M. Groeneveld H. Zhang J. W. Verhoeven J. Am. Chem. Soc. 2005 127 16054
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 16054
- Benniston, A.C.¹ Harriman, A.² Li, P.³ Rostron, J.P.⁴ Van Ramesdonk, H.J.⁵ Groeneveld, M.M.⁶ Zhang, H.⁷ Verhoeven, J.W.⁸

18
- 43949133851
- 3MLCT luminescence lifetime of 4 See details of the calculation in the ESI
- Z. E. X. Dance S. M. Mickley T. M. Wilson A. B. Ricks A. M. Scott M. A. Ratner M. R. Wasielewski J. Phys. Chem. A 2008 112 4194
- (2008) J. Phys. Chem. a , vol.112 , pp. 4194
- Dance, Z.E.X.¹ Mickley, S.M.² Wilson, T.M.³ Ricks, A.B.⁴ Scott, A.M.⁵ Ratner, M.A.⁶ Wasielewski, M.R.⁷

19
- 0033526308
- 1MLCT bands in 4 are expected to be slightly different than the sum of the individual separated components, on the basis of comparisons of the spectra of 1, 3, and 4 in Fig. 2. This, together with experimental uncertainty of the quantum yield (20%) can justify the difference (50% vs. 28%) in the theoretical and experimental reduction of emission quantum yields of singlet bodipy emission on passing from 510 to 435 nm excitation
- B. Schlicke P. Belser L. De Cola E. Sabbioni V. Balzani J. Am. Chem. Soc. 1999 121 4207
- (1999) J. Am. Chem. Soc. , vol.121 , pp. 4207
- Schlicke, B.¹ Belser, P.² De Cola, L.³ Sabbioni, E.⁴ Balzani, V.⁵

20
- 1442360836
- J. Andersson F. Puntoriero S. Serroni A. Yartsev T. Pascher T. Polivka S. Campagna V. Sundström Chem. Phys. Lett. 2004 386 336
- (2004) Chem. Phys. Lett. , vol.386 , pp. 336
- Andersson, J.¹ Puntoriero, F.² Serroni, S.³ Yartsev, A.⁴ Pascher, T.⁵ Polivka, T.⁶ Campagna, S.⁷ Sundström, V.⁸

21
- 33744534947
- F. N. Castellano I. E. Pometschenko E. Shikhova F. Hua M. L. Muro N. Rajapakse Coord. Chem. Rev. 2006 250 1819
- (2006) Coord. Chem. Rev. , vol.250 , pp. 1819
- Castellano, F.N.¹ Pometschenko, I.E.² Shikhova, E.³ Hua, F.⁴ Muro, M.L.⁵ Rajapakse, N.⁶

22
- 0004122810
- V. Balzani, Wiley-VCH, Weinheim, p. 179
- M. N. Paddon-Row, in Electron Transfer in Chemistry, ed., V. Balzani,, Wiley-VCH, Weinheim, 2001, vol. 3, p. 179
- (2001) Electron Transfer in Chemistry, Ed.
- Paddon-Row In, M.N.¹

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