Abstract
In this chapter we discuss some of the typical materials used in photochemistry. We describe, in general terms, how their suitability for application as absorber, emitter, sensitiser, energy acceptor or quencher, depends on the energy states within the material and the routes of interconversion between these states, and also how suitability as a redox or chemical sensitiser/acceptor/trap is determined by specific chemical reactivities. We describe the application of photochemical principles to the design of light sources and displays, and describe the photochemical principles and applications of photochromics and molecular switches. A table giving the structures, characteristics, and uses, of a number of compounds widely used in photochemistry is provided at the end of the chapter.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Griffiths J (1976) Colour and constitution of organic molecules. Academic Press, London
Christie RM (2001) Colour chemistry. Royal Society of Chemistry, Cambridge
Tilley R (2011) Colour and the optical properties of materials, 2nd edn. Wiley, Chichester
Reinen D, Lindner G–G (1999) The nature of the chalcogen colour centres in ultramarine-type solids. Chem Soc Rev 28:75–84
Ball P (2002) Bright earth, the invention of colour. Penguin, London
Głowacki ED, Voss G, Leonat L et al (2012) Indigo and tyrian purple—from ancient natural dyes to modern organic semiconductors. Israel J Chem 52:540–551
Nozik AJ, Beard MC, Luther JM et al (2010) Semiconductor quantum dots and quantum dot arrays and applications of multiple exciton generation to third-generation photovoltaic solar cells. Chem Rev 110:6873–6890
Cox J (2003) A quantum paintbox. Chem Br 39:21–25
Booth K, Hill S (1998) The essence of optoelectronics. Prentice Hall, London
Webb AR (2006) Considerations for lighting in the built environment: non-visual effects of light. Energy Build 38:721–727
Lister GG, Lawler JE, Lapatovich WP, Godyak VA (2004) The physics of discharge lamps. Rev Mod Phys 76:541–598
Leverenz HW (1949) Luminescent solids (phosphors). Science 109:183–195
Feldmann C, Jüstel T, Ronda C, Schmidt PJ (2003) Inorganic luminescent materials: 100 years of research and applications. Adv Funct Mater 13:511–516
Levine AK, Palilla FC (1964) New highly efficient red-emitting cathodoluminescent phosphor (YVO4-Eu) for color television. Appl Phys Lett 5:118–120
Commission Internationale de L’Éclairage (CIE) (1986) Colorimetry. Publication Report No. 15.2, IEC/CIE, Vienna
Fairman HS, Brill MH, Hemmendinger H (1997) How the CIE color-matching functions were derived from Wright-Guild data. Color Res Appl 22:11–23
Jüstel T, Nikol H, Ronda C (1998) New developments in the field of luminescent materials for lighting and displays. Angew Chem Int Ed 37:3084–3103
Förster T (1959) Transfer mechanisms of electronic excitation. Disc Faraday Soc 27:7–17
Dexter DL (1953) A theory of sensitized luminescence in solids. J Chem Phys 21:836–850
Bürmen M, Pernuš F, Likar B (2008) LED light sources: a survey of quality-affecting factors and methods for their assessment. Meas Sci Technol 19:122002
Schadt M (2009) Milestone in the history of field-effect liquid crystal displays and materials. Japan J Appl Phys 48:03B001
Eden JG (2006) Information display early in the 21st century: overview of selected emissive display technologies. Proc IEEE 94:567–574
Hung LS, Chen CH (2002) Recent progress of organic electroluminescent materials and devices. Mater Sci Eng R 39:143–222
Bamfield P (2001) Chromic phenomena. Royal Society of Chemistry, Cambridge
Steranka FM, Bhat J, Collins D et al (2002) High power LEDs—technology status and market applications. Phys Stat Sol (a) 194:380–388
Dupuis TD, Krames MR (2008) History, development, and applications of high-brightness visible light-emitting diodes. J Lightwave Technol 26:1154–1171
Holonyak N, Bevacqua SF (1962) Coherent (visible) light emission from Ga(As1−xPx) junctions. Appl Phys Lett 1:82–83
Nakamura S, Mukai T, Senoh M (1994) Candela-class high brightness InGaN/AlGaN double heterostructure blue light emitting diodes. Appl Phys Lett 64:1687–1689
Ye S, Xiao F, Pan YX et al (2010) Phosphors in phosphor-converted white light-emitting diodes: recent advances in materials, techniques and properties. Mater Sci Eng R 71:1–34
Grandjean N (2010) LED light sources (light for the future). J Phys D Appl Phys 43:350301 and following articles
Salbeck J (1996) Electroluminescence with organic compounds. Ber Bunsenges Phys Chem 100:1667–1677
Tang CW (1982) Organic electroluminescent cell. U.S. Patent Number 4,356,429 (Eastman Kodak Company)
Friend RH, Burroughes JH, Bradley DD (1993) Electroluminescent devices. U.S. Patent Number 5,247,190 (Cambridge Research and Innovation Limited)
Friend RH, Gymer RW, Holmes AB et al (1999) Electroluminescence in conjugated polymers. Nature 397:121–128
Grimsdale AC, Chan KL, Martin RE et al (2009) Synthesis of light-emitting conjugated polymers for applications in electroluminescent devices. Chem Rev 109:897–1091
Thompson ME, Burrows PE, Forrest SR (1999) Electrophosphorescence in organic light emitting diodes. Curr Opin Solid State Mater Sci 4:369–372
D’Andrade BW, Forrest SR (2004) White organic light-emitting devices for solid-state lighting. Adv Mater 16:1585–1595
Evans RC, Douglas P, Winscom CJ (2006) Coordination complexes exhibiting room temperature phosphorescence: evaluation of their suitability as triplet emitters in organic light emitting diodes. Coord Chem Rev 250:2093–2126
Kamtekar KT, Monkman AP, Bryce MR (2009) Recent advances in white organic light-emitting materials and devices (WOLEDS). Adv Mater 22:572–582
Liu B, Bazan GC (2004) Homogeneous fluorescence-based DNA detection with water-soluble conjugated polymers. Chem Mater 16:4467–4476
Davies ML, Douglas P, Burrows HD et al (2011) Effect of aggregation on the photophysical properties of three fluorene–phenylene-based cationic conjugated polyelectrolytes. J Phys Chem B 115:6885–6892
Thomas SW, Joly GD, Swager TM (2007) Chemical sensors based on amplifying fluorescent conjugated polymers. Chem Rev 107:1339–1386
Achyuthan KE, Bergstedt TS, Chen L et al (2005) Fluorescence superquenching of conjugated polyelectrolytes: applications for biosensing and drug discovery. J Mater Chem 15:2648–2656
Coakley KM, McGehee MD (2004) Conjugated polymer photovoltaic cells. Chem Mater 16:4533–4542
Montalti M, Credi A, Prodi L, Gandolfi MT (2006) Handbook of photochemistry, 3rd edn. CRC Press, New York
Balzani V, Bolletta F, Scandola F (1980) Vertical and nonvertical energy transfer processes. A general classical treatment. J Am Chem Soc 102:2152–2163
Lehn J-M (1990) Perspectives in supramolecular chemistry—from molecular recognition towards molecular information processing and self-organization. Angew Chem Int Ed 29:1304–1319
Wilkinson F, Helman WP, Ross AB (1995) Rate constants for the decay and reaction of the lowest electronically excited singlet state of molecular oxygen in solution. An expanded and revised compilation. J Phys Chem Ref Data 24:663–677
Wilkinson F, Brummer JG (1981) Rate constants for the decay and reaction of the lowest electronically excited singlet state of molecular oxygen in solution. J Phys Chem Ref Data 10:809–999
Henbest K, Douglas P, Garley MS, Mills A (1994) Persulphate quenching of the excited state of ruthenium(II) tris-bipyridyl dication: thermal reactions. J Photochem Photobiol A Chem 80:299–305
Bouas-Laurent H, Dürr H (2001) Organic photochromism (IUPAC technical report). Pure Appl Chem 73:639–665
Olive AGL, Del Guerzo A, Pozzo J-L, Desvergne J-P (2007) Photoimerization of soluble tetracene derivatives using visible light. J Phys Org Chem 20:838–844
Hirshberg Y (1950) Photochromie dans la serie de la bianthrone. Compt Rend Acad Sci 231:903–904
Brown GH (ed) (1971) Photochromism. Wiley-Interscience, New York
Smith GP (1967) Photochromic glasses: properties and applications. J Mater Sci 2:139–152
Armistead WH, Stookey SD (1964) Photochromic silicate glasses sensitized by silver halides. Science 144:150–154
Crano JC, Flood T, Knowles D et al (1996) Photochromic compounds: chemistry and application in ophthalmic lenses. Pure Appl Chem 68:1395–1398
Corns SN, Partington SM, Towns A (2009) Industrial organic photochromic dyes. Color Technol 125:249–261
Dürr H, Bouas-Laurent H (eds) (1990) Photochromism: molecules and systems. Elsevier, Amsterdam
Crano JC, Guglielmetti RJ (eds) (2001) Organic photochromic and thermochromic compounds, vols 1 and 2. Plenum, New York
Irie M (2000) Photochromism: memories and switches. Chem Rev 100:1683 and following articles
Favaro G, Irie M (eds) (2011) Special issue on photochromism. J Photochem Photobiol C 12:71–236
Wyman GM (1955) The cis-trans isomerization of conjugated compounds. Chem Rev 55:625–657
Zimerman G, Chow LY, Paik UJ (1958) The photochemical isomerization of azobenzene. J Am Chem Soc 80:3528–3531
Ercole F, Davis TP, Evans RA (2010) Photo-responsive systems and biomaterials: photochromic polymers, light-triggered self-assembly, surface modification, fluorescence modulation and beyond. Polym Chem 1:37–54
Hampp N (2000) Bacteriorhodopsin as a photochromic retinal protein for optical memories. Chem Rev 100:1755–1776
Matsuda K, Irie M (2004) Diarylethene as a photoswitching unit. J Photochem Photobiol C 5:169–182
Yokoyama Y (2000) Fulgides for memories and switches. Chem Rev 100:1717–1739
Corval A, Kuldová K, Eichen Y et al (1996) Photochromism and thermochromism driven by intramolecular proton transfer in dinitrobenzylpyridine compounds. J Phys Chem 100:19315–19320
Naumov P (2006) Photochromism of ortho-nitrobenzylpyridines: a brief overview. J Mol Struct 783:1–8
Irie M, Miyatake O, Uchida K (1992) Blocked photochromism of diarylethenes. J Am Chem Soc 114:8715–8716
Pina F, Petrov V, Laia CAR (2012) Photochromism of flavylium systems. An overview of a versatile multistate system. Dyes Pigments 92:877–889
Uchida M, Irie M (1993) Two-photon photochromism of a naphthopyran derivative. J Am Chem Soc 115:6442–6443
Parthenopoulos DA, Rentzepis PM (1989) Three-dimensional optical storage memory. Science 245:843–845
Towns A (2012) Olympian colour chemistry. Chem Ind 76:32–35
Wang PY, Wu CJ (1997) Photochromic behavior of some phenoxyanthroquinone dyes in solution and on polyester substrate. Dyes Pigments 35:279–288
Cheng T, Lin T, Brady R, Wang X (2008) Photochromic fabrics with improved durability and photochromic performance. Fibers Polym 9:521–526
Moore GE (1965) Cramming more components onto integrated circuits. Electronics 38:4–7
Kawata S, Kawata Y (2000) Three-dimensional optical data storage using photochromic materials. Chem Rev 100:1777–1788
Tsujioka T, Irie M (1998) Fluorescence readout of near-field photochromic memory. Appl Opt 115:119458–119460
Balzani V, Credi A, Venturi M (2008) Molecular devices and machines. Concepts and perspectives. Wiley-VCH, Weinheim
Natali M, Giordani S (2012) Molecular switches as photocontrollable “smart” receptors. Chem Soc Rev 41:4010–4029
de Silva AP, McClenaghan ND (2004) Molecular-scale logic gates. Chem Eur J 10:574–586
http://www.zyvex.com/nanotech/feynman.html. Accessed 25 August 2012
Feringa BL (ed) (2001) Molecular switches. Wiley-VCH, Weinheim
Feringa BL (2001) In control of motion: from molecular switches to molecular motors. Acc Chem Res 34:504–513
Russew M–M, Hecht S (2010) Photoswitches: from molecules to materials. Adv Mater 22:3348–3360
Balzani V, Credi A, Venturi M (2009) Light powered molecular machines. Chem Soc Rev 38:1542–1550
Leo WR (ed) (1994) Techniques for nuclear and particle physics experiments, 2nd edn. Springer, Berlin
Hepp A, Heil H, Weise W et al (2003) Light-emitting field-effect transistor based on a tetracene thin film. Phys Rev Lett 91:406–410
Takahashi T, Takenobul T, Takeya J, Iwasa Y (2007) Ambipolar light-emitting transistors of a tetracene single crystal. Adv Funct Mater 17:1623–1628
Katraro R, Ron A, Speiser S (1979) Photophysical studies of coronene and 1,12-benzperylene. Self-quenching, photoquenching, temperature dependent fluorescence decay and temperature dependent electronic energy transfer to dye acceptors. Chem Phys 42:121–132V
Glushko V, Thaler MSR, Karp CD (1981) Pyrene fluorescence fine structure as a polarity probe of hydrophobic regions: behavior in model solvents. Arch Biochem Biophys 210:33–42
Lakowicz JR, Knutson JR (1980) Hindered depolarizing rotations of perylene in lipid bilayers. Detection by lifetime-resolved fluorescence anisotropy measurements. Biochemistry 19:905–911
Armstrong N, Wightman M, Gross E (2001) Light-emitting electrochemical processes. Annu Rev Phys Chem 52:391–422
Hoven CV, Garcia A, Bazan GC, Nguyen TQ (2008) Recent applications of conjugated polyelectrolytes in optoelectronic devices. Adv Mater 20:3793–3810
Vaschetto ME, Monkman AP, Springborg M (1999) First-principles studies of some conducting polymers: PPP, PPy, PPV, PPyV, and PANI. J Mol Struct Theochem 468:181–191
Rehahn M, Schlüter AD, Wegner G (1990) Soluble poly(para-phenylene)s 3. Variation of the length and the density of the solubilizing side chains. Makromol Chem 191:1991–2003
Yang Y, Pei Q, Heeger AJ (1996) Efficient blue polymer light-emitting diodes from a series of soluble poly(paraphenylene)s. J Appl Phys 79:934–939
Burroughes JH, Bradley DDC, Brown AR et al (1990) Light-emitting diodes based on conjugated polymers. Nature 347:539–541
Li J, Sun N, Guo ZX et al (2002) Photovoltaic devices with methanofullerenes as electron acceptors. J Phys Chem B 106:11509–11514
Grüner JF, Hamer P, Friend RH et al (1994) A high efficiency blue-light-emitting diode based on novel ladder poly(p-phenylene)s. Adv Mater 6:748–752
Li Z, Meng H (eds) (2007) Organic light-emitting materials and devices. CRC Press, New York
Takahashi K, Seto K, Yamaguchi T et al (2004) Performance enhancement by blending an electron acceptor in TiO2/polyphenylenevinylene/Au solid-state solar cells. Chem Lett 33:1042–1043
Yang M, Zhang Q (2004) Organic light emitting diodes based on multi-wall carbon nanotubes (MWNTs) modified electrode. J Mater Sci 39:3777–3778
Shen F, He F, Lu D et al (2006) Bright and colour stable white polymer light-emitting diodes. Semi Sci Tech 22:L16–L19
Moses D (1993) High quantum efficiency luminescence from a conducting polymer in solution: a polymer laser dye. Synth Met 55:22–27
Chen L, McBranch DW, Wang HL et al (1999) Highly sensitive biological and chemical sensors based on reversible fluorescence quenching in a conjugated polymer. Proc Nat Acad Sci USA 96:12287–12292
Gerard M, Chaubey A, Malhotra BD (2002) Application of conducting polymers to biosensors. Biosens Bioelectron 17:345–359
Scherf U, Neher D (eds) (2008) Polyfluorenes: Advances in Polymer Science. Springer, Berlin
Davies ML, Burrows HD, Morán MC et al (2009) Cationic fluorene-based conjugated polyelectrolytes induce compaction and bridging in DNA. Biomacromolecules 10:2987–2997
Liu B, Bazan GC (2004) Homogeneous fluorescence-based DNA detection with water-soluble conjugated polymers. Chem Mater 16:4467–4476
Garnier F (1998) Field-effect transistors based on conjugated materials. In: Müllen K, Wegner G (eds) Electronic materials: the oligomer approach. Wiley-VCH, Weinheim
Tsiminis G, Ruseckas A, Samuel IDW, Turnbull GA (2009) A two-photon pumped polyfluorene laser. Appl Phys Lett 94:253304-1-253304-3
Price S, Stuart A, Yang L, Zhou H (2011) Fluorine substituted conjugated polymer of medium band gap yields 7% efficiency in polymer–fullerene solar cells. J Am Chem Soc 133:4625–4631
Scheinert S, Doll T, Scherer A et al (2004) Organic field-effect transistors with nonlithographically defined submicrometer channel length. Appl Phys Lett 84:4427–4429
Landi BJ, Raffaelle RP, Castro SL, Bailey SG (2005) Single-wall carbon nanotube–polymer solar cells. Prog Photovolt Res Appl 13:165–172
Do H, Reinhard M, Vogeler H et al (2009) Polymeric anodes from poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) for 3.5% efficient organic solar cells. Thin Solid Films 517:5900–5902
Kubin RF, Fletcher AN (1982) Fluorescence quantum yields of some rhodamine dyes. J Lumin 27:455–462
Casey KG, Quitevis EL (1988) Effect of solvent polarity on nonradiative processes in xanthene dyes: Rhodamine B in normal alcohols. J Phys Chem 92:6590–6594
Schäfer FP (1990) Dye lasers, 3rd edn. Springer, Berlin
Duarte FJ, Hillman LW (1990) Dye laser principles. Academic, New York
De Bernardo S, Weigele M, Toome V et al (1974) Studies on the reaction of fluorescamine with primary amines. Arch Biochem Biophys 163:390
DeRosa MC, Crutchley RJ (2002) Photosensitized singlet oxygen and its application. Coord Chem Rev 233–234:351–371
Seybold PG, Gouterman M, Callis J (1969) Calometric, photometric and lifetime determinations of fluorescence yields of fluorescein dyes. Photochem Photobiol 9:229–242
Johnson I, Spence MTZ, Molecular probes handbook—a guide to fluorescent probes and labelling technologies, 11th edn. Life Technologies, Carlsbad
Noukakis D, Auweraer MV, Toppet S, De Schryver FC (1995) Photophysics of thiacarbocyanine dye in organic solvent. J Phys Chem 99:11860–11866
Jabbour GE, Wang JF, Peyghambarian N (2002) High-efficiency organic electrophophorescent devices through balance of charge injection. Appl Phys Lett 80:2026–2028
Barnett GH, Hudson MF, Smith KM (1975) Concerning meso-tetraphenylporphyrin purification. J Chem Soc Perkin Trans 1 1401–1403
Strachan JP, Gentemann S, Seth J et al (1997) Effects of orbital ordering on electronic communication in multiporphyrin arrays. J Am Chem Soc 119:11191–11201
Baldo MA, O’Brien DF, You Y et al (1998) Highly efficient phosphorescent emission from organic electroluminescent devices. Nature 395:151–154
Cleave V, Yahioglu G, Barny PL et al (1999) Harvesting singlet and triplet energy in polymer LEDs. Adv Mater 11:285–288
Whalley M (1961) Conjugated macrocycles. Part XXXII. Absorption spectra of tetrazaporphins and phthalocyanines. Formation of pyridine salts. J Chem Soc 866–869
Tang CW (1986) Two‐layer organic photovoltaic cell. Appl Phys Lett 48:183–185
Pfuetzner S, Meiss J, Petrich A et al (2009) Thick C60:ZnPc bulk heterojunction solar cells with improved performance by film deposition on heated substrates. Appl Phys Lett 94:253303-1–253303-3
Kumar GA, Santhosh C (2003) Spectral studies and radiative characteristics of naphthalocyanine molecules in DMF. Mater Lett 57:2315–2319
Tang CW, Van Slyke SA (1987) Organic electroluminescent diodes. Appl Phys Lett 51:913–915
Hoshi T, Kumagai K, Inoue K et al (2008) Electronic absorption and emission spectra of Alq3 in solution with special attention to a delayed fluorescence. J Lumin 128:1353–1358
O’Regan B, Grätzel M (1991) A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films. Nature 335:737–740
Nazeeruddin MK, De Angelis F, Fantacci S et al (2005) Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers. J Am Chem Soc 127:16835–16847
Nazeeruddin MK, Péchy P, Renouard T et al (2001) Engineering of efficient panchromatic sensitizers for nanocrystalline TiO2-based solar cells. J Am Chem Soc 123:1613–1624
Deaton JC, Young RH, Lenhard JR et al (2010) Photophysical properties of the series fac- and mer-(1-phenylisoquinolinato-NC2′)(x)(2-phenylpyridinato-NC2′)3 − x iridium(III) (x = 1–3). Inorg Chem 49:9151–9161
Fischer H, Baer R, Hany R et al (1990) 2,2-Dimethoxy-2-phenylacetophenone: photochemistry and free radical photofragmentation. J Chem Soc Perkin Trans 2 (5):787–798
Iwamoto S, Kai W, Isogai T et al (2010) Comparison study of TEMPO-analogous compounds on oxidation efficiency of wood cellulose for preparation of cellulose nanofibrils. Polym Degrad Stabil 95:1394–1398
Kamibayashi M, Oowada S, Kameda H et al (2006) Synthesis and characterization of a practically better DEPMPO-type spin trap, 5-(2,2-dimethyl-1,3-propoxy cyclophosphoryl)-5-methyl-1-pyrroline N-oxide (CYPMPO). Free Radic Res 40:1166–1172
Dambrova M, Baumanea L, Kalvinsha I, Wikberg JES (2000) Improved method for EPR detection of DEPMPO-superoxide radicals by liquid nitrogen freezing. Biochem Biophys Res Commun 275:895–898
Hagfeldt A, Boschloo G, Sun L et al (2010) Dye-sensitized solar cells. Chem Rev 110:6595–6663
Zhang XT, Liu YC, Zhi ZZ et al (2002) Temperature dependence of excitonic luminescence from nanocrystalline ZnO films. J Lumin 99:149–154
Reynolds D, Leies G, Antes L, Marburger R (1954) Photovoltaic effect in cadmium sulfide. Phys Rev 96:533–534
Bube RH (1955) Temperature dependence of the width of the band gap in several photoconductors. Phys Rev 98:431–433
Mali SS, Desai SK, Kalagi SS et al (2012) PbS quantum dot sensitized anatase TiO2 nanocorals for quantum dot-sensitized solar cell applications. Dalton Trans 41:6130–6136
Zhang S, Nakai Y, Tsuboi T et al (2011) The thermal stabilities of luminescence and microstructures of Eu2+-doped KBaPO4 and NaSrPO4 with β-K2SO4 type structure. Inorg Chem 50:2897–2904
Lu J, Yagi H, Takaichi K et al (2004) 110 W ceramic Nd3+: Y3Al5O12 laser. Appl Phys B 79:25–28
Vielhaber G, Grether-Beck S, Koch O et al (2006) Sunscreens with an absorption maximum of ≥360 nm provide optimal protection against UVA1-induced expression of matrix metalloproteinase-1, interleukin-1, and interleukin-6 in human dermal fibroblasts. Photochem Photobiol Sci 5:275–282
Zechmeister L, Polgar A (1943) Cis-trans isomerization and spectral characteristics of carotenoids and some related compounds. J Am Chem Soc 65:1522–1528
Naguiba YMA, Steel C, Young MA (2001) Decay kinetics of photosensitized triplet crystal violet in acetonitrile. J Photochem Photobiol A-Chem 141:33–38
Tuite EM, Kelly JM (1993) New trends in photobiology: photochemical interactions of methylene blue and analogues with DNA and other biological substrates. J Photochem Photobiol B-Biol 21:103–124
Pattanaargson S, Munhapol T, Hirunsupachot P, Luangthongaram P (2004) Photoisomerization of octyl methoxycinnamate. J Photochem Photobiol A-Chem 161:269–274
Reichardt C (1994) Solvatochromic dyes as solvent polarity indicators. Chem Rev 94:231–2358
Holliman PJ, Davies ML, Connell A et al (2010) Ultra-fast dye sensitisation and co-sensitisation for dye sensitized solar cells. Chem Commun 46:7256–7258
Ho CJ, Motyka AL, Topp MR (1989) Picosecond time-resolved S2 → S0 fluorescence of xanthione in different fluid solvents. Chem Phys Lett 158:51–59
Seefeldt B, Kasper R, Beining M et al (2010) Spiropyrans as molecular optical switches. Photochem Photobiol Sci 9:213–220
Landgraf JK, Braun M, Özçoban C et al (2012) Ultrafast dynamics of a spiropyran in water. J Am Chem Soc 134:14070–14077
Chibisov AK, Görner H (2001) Photochromism of spirobenzopyranindolines and spironaphthopyranindolines. Phys Chem Chem Phys 3:424–431
Ercole F, Malic N, Davis TP, Evans RA (2009) Optimizing the photochromic performance of naphthopyrans in a rigid host matrix using poly(dimethylsiloxane) conjugation. J Mater Chem 19:5612–5623
Gray GW, Kelly SM (1999) Liquid crystals for twisted nematic display devices. J Mater Chem 9:2037–2050
Lumileds Corporation (2004) Luxeon Reliability. Application Brief AB25 11
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer Science+Business Media Dordrecht
About this chapter
Cite this chapter
Davies, M.L., Douglas, P., Evans, R.C., Burrows, H.D. (2013). Photochemical Materials: Absorbers, Emitters, Displays, Sensitisers, Acceptors, Traps and Photochromics. In: Evans, R., Douglas, P., Burrow, H. (eds) Applied Photochemistry. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-3830-2_4
Download citation
DOI: https://doi.org/10.1007/978-90-481-3830-2_4
Published:
Publisher Name: Springer, Dordrecht
Print ISBN: 978-90-481-3829-6
Online ISBN: 978-90-481-3830-2
eBook Packages: Chemistry and Materials ScienceChemistry and Material Science (R0)