Abstract
Fostered by the success of photodynamic therapy (PDT), light activation of transition metal complexes has raised notable interest for applications in biology and in medicine. The rich photochemistry of metal complexes and the arsenal of chemical reactions accessible via light excitation have been exploited for developing therapeutic agents which exert their biological action through novel mechanisms. This chapter aims to provide an overview of the concepts and strategies adopted by leading scientists in the design and development of photoactivatable metal complexes with potential use in cancer therapy. In particular, we focus on the anticancer properties of Pt, Rh, and Ru complexes which have been demonstrated to be amongst the most promising classes of compounds.
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References
Felsher DW (2003) Opinion: cancer revoked: oncogenes as therapeutic targets. Nat Rev Cancer 3:375–379
Bown SG (2013) Photodynamic therapy for photochemists. Philos Trans R Soc Math Phys Eng Sci 371:20120371
Schatzschneider U (2010) Photoactivated biological activity of transition-metal complexes. Eur J Inorg Chem 2010:1451–1467
DeRosa MC, Crutchley RJ (2002) Photosensitized singlet oxygen and its applications. Coord Chem Rev 233:351–371
Naik A, Rubbiani R, Gasser G, Spingler B (2014) Visible-light-induced annihilation of tumor cells with platinum-porphyrin conjugates. Angew Chem Int Ed 53:6938–6941
Sun Y, Joyce LE, Dickson NM, Turro C (2010) DNA photocleavage by an osmium(II) complex in the PDT window. Chem Commun 46:6759–6761
Farrer NJ, Salassa L, Sadler PJ (2009) Photoactivated chemotherapy (PACT): the potential of excited-state d-block metals in medicine. Dalton Trans 48:10690–10701
Elias B, Kirsch-De Mesmaeker A (2006) Photo-reduction of polyazaaromatic Ru(II) complexes by biomolecules and possible applications. Coord Chem Rev 250:1627–1641
Fino E, Araya R, Peterka DS, Salierno M, Etchenique R, Yuste R (2009) RuBi-glutamate: two-photon and visible-light photoactivation of neurons and dendritic spines. Front Neural Circuits 3:1–9
Salierno M, Marceca E, Peterka DS, Yuste R, Etchenique R (2010) A fast ruthenium polypyridine cage complex photoreleases glutamate with visible or IR light in one and two photon regimes. J Inorg Biochem 104:418–422
Zayat L, Calero C, Alborés P, Baraldo L, Etchenique R (2003) A new strategy for neurochemical photodelivery: metal–ligand heterolytic cleavage. J Am Chem Soc 125:882–883
Niesel J, Pinto A, Peindy N’Dongo HW, Merz K, Ott I, Gust R, Schatzschneider U (2008) Photoinduced CO release, cellular uptake and cytotoxicity of a tris(pyrazolyl)methane (tpm) manganese tricarbonyl complex. Chem Commun 15:1798–1800
Rose MJ, Fry NL, Marlow R, Hinck L, Mascharak PK (2008) Sensitization of ruthenium nitrosyls to visible light via direct coordination of the dye resorufin: trackable NO donors for light-triggered NO delivery to cellular targets. J Am Chem Soc 130:8834–8846
Ford PC (2008) Polychromophoric metal complexes for generating the bioregulatory agent nitric oxide by single- and two-photon excitation. Acc Chem Res 41:190–200
Fry NL, Mascharak PK (2011) Photoactive ruthenium nitrosyls as NO donors: how to sensitize them toward visible light. Acc Chem Res 44:289–298
Schatzschneider U (2011) PhotoCORMs: light-triggered release of carbon monoxide from the coordination sphere of transition metal complexes for biological applications. Inorg Chim Acta 374:19–23
Zayat L, Filevich O, Baraldo LM, Etchenique R (2013) Ruthenium polypyridyl phototriggers: from beginnings to perspectives. Philos Trans R Soc Math Phys Eng Sci 371:20120330
Rosenberg B, Van Camp L, Grimley EB, Thomson AJ (1967) The inhibition of growth or cell division in Escherichia coli by different ionic species of platinum (IV) complexes. J Biol Chem 242:1347–1352
Wheate NJ, Walker S, Craig GE, Oun R (2010) The status of platinum anticancer drugs in the clinic and in clinical trials. Dalton Trans 39:8113–8127
Kratochwil NA, Bednarski PJ, Mrozek H, Vogler A, Nagle JK (1996) Photolysis of an iodoplatinum(IV) diamine complex to cytotoxic species by visible light. Anticancer Drug Des 11:155–171
Kratochwil NA, Zabel M, Range K-J, Bednarski PJ (1996) Synthesis and X-ray crystal structure of trans, cis-[Pt(OAc)2I2(en)]: a novel type of cisplatin analog that can be photolyzed by visible light to DNA-binding and cytotoxic species in vitro. J Med Chem 39:2499–2507
Garino C, Salassa L (2013) The photochemistry of transition metal complexes using density functional theory. Philos Trans R Soc Math Phys Eng Sci 371:20120134
Kratochwil NA, Parkinson JA, Bednarski PJ, Sadler PJ (1999) Nucleotide platination induced by visible light. Angew Chem Int Ed 38:1460–1463
Vogler A, Kern A, Fusseder BZ (1978) M-azide photochemistry. Naturforsch B 33:1352–1356
Vogler A, Hlavatsch J (1983) M-azide photochemistry second article. Angew Chem Int Ed Engl 22:154–155
Muller P, Schroder B, Parkinson JA, Kratochwil NA, Coxall RA, Parkin A, Parsons S, Sadler PJ (2003) Nucleotide cross-linking induced by photoreactions of platinum(IV) azide complexes. Angew Chem Int Ed 42:335–339
Mackay FS, Woods JA, Moseley H, Ferguson J, Dawson A, Parsons S, Sadler PJ (2006) A photoactivated trans-diammine platinum complex as cytotoxic as cisplatin. Chem Eur J 12:3155–3161
Kašpárková J, Mackay FS, Brabec V, Sadler PJ (2003) Formation of platinated GG cross-links on DNA by photoactivation of a platinum(IV) azide complex. J Biol Inorg Chem 8:741–745
Ronconi L, Sadler PJ (2008) Unprecedented carbon–carbon bond formation induced by photoactivation of a platinum(IV)-diazido complex. Chem Commun 2:235–237
Phillips HIA, Ronconi L, Sadler PJ (2009) Photoinduced reactions of cis, trans, cis-[Pt(IV)(N3)2(OH)2(NH3)2] with 1-methylimidazole. Chem Eur J 15:1588–1596
Heringova P, Woods J, Mackay FS, Kasparkova J, Sadler PJ, Brabec V (2006) Transplatin is cytotoxic when photoactivated: enhanced formation of DNA cross-links. J Med Chem 49:7792–7798
Westendorf AF, Bodtke A, Bednarski PJ (2011) Studies on the photoactivation of two cytotoxic trans, trans, trans-diazidodiaminodihydroxo-Pt(IV) complexes. Dalton Trans 40:5342–5351
Bednarski PJ, Grünert R, Zielzki M, Wellner A, Mackay FS, Sadler PJ (2006) Light-activated destruction of cancer cell nuclei by platinum diazide complexes. Chem Biol 13:61–67
Mackay FS, Woods JA, Heringová P, Kašpárková J, Pizarro AM, Moggach SA, Parsons S, Brabec V, Sadler PJ (2007) A potent cytotoxic photoactivated platinum complex. Proc Natl Acad Sci U S A 104:20743–20748
Farrer NJ, Woods JA, Salassa L, Zhao Y, Robinson KS, Clarkson G, Mackay FS, Sadler PJ (2010) A potent trans-diimine platinum anticancer complex photoactivated by visible light. Angew Chem Int Ed 49:8905–8908
Westendorf AF, Zerzankova L, Salassa L, Sadler PJ, Brabec V, Bednarski PJ (2011) Influence of pyridine versus piperidine ligands on the chemical, DNA binding and cytotoxic properties of light activated trans, trans, trans-[Pt(N3)2(OH)2(NH3)(L)]. J Inorg Biochem 105:652–662
Westendorf AF, Woods JA, Korpis K, Farrer NJ, Salassa L, Robinson K, Appleyard V, Murray K, Grünert R, Thompson AM, Sadler PJ, Bednarski PJ (2012) Trans, trans, trans-[PtIV(N3)2(OH)2(py)(NH3)]: a light-activated antitumor platinum complex that kills human cancer cells by an apoptosis-independent mechanism. Mol Cancer Ther 11:1894–1904
Butler JS, Woods JA, Farrer NJ, Newton ME, Sadler PJ (2012) Tryptophan switch for a photoactivated platinum anticancer complex. J Am Chem Soc 134:16508–16511
Pracharova J, Zerzankova L, Stepankova J, Novakova O, Farrer NJ, Sadler PJ, Brabec V, Kasparkova J (2012) Interactions of DNA with a new platinum(IV) azide dipyridine complex activated by UVA and visible light: relationship to toxicity in tumor cells. Chem Res Toxicol 25:1099–1111
Zhao Y, Woods JA, Farrer NJ, Robinson KS, Pracharova J, Kasparkova J, Novakova O, Li H, Salassa L, Pizarro AM, Clarkson GJ, Song L, Brabec V, Sadler PJ (2013) Diazido mixed-amine platinum(IV) anticancer complexes activatable by visible-light form novel DNA adducts. Chem Eur J 19:9578–9591
Mackay FS, Farrer NJ, Salassa L, Tai HC, Deeth RJ, Moggach SA, Wood PA, Parsons S, Sadler PJ (2009) Synthesis, characterisation and photochemistry of PtIV pyridyl azido acetato complexes. Dalton Trans 13:2315–2325
Mackay FS, Moggach SA, Collins A, Parsons S, Sadler PJ (2009) Photoactive trans ammine/amine diazido platinum(IV) complexes. Inorg Chim Acta 362:811–819
Farrer NJ, Woods JA, Munk VP, Mackay FS, Sadler PJ (2010) Photocytotoxic trans-diam(m)ine platinum(IV) diazido complexes more potent than their cis isomers. Chem Res Toxicol 23:413–421
Cubo L, Pizarro AM, Quiroga AG, Salassa L, Navarro-Ranninger C, Sadler PJ (2010) Photoactivation of trans diamine platinum complexes in aqueous solution and effect on reactivity towards nucleotides. J Inorg Biochem 104:909–918
Howard RA, Kimball AP, Bear JL (1979) Mechanism of action of tetra-μ-carboxylatodirhodium(II) in L1210 tumor suspension culture. Cancer Res 39:2568–2573
Zyngier S, Kimura E, Najjar R (1989) Antitumor effects of rhodium-(II) citrate in mice bearing Ehrlich tumors. Braz J Med Biol Res 22:397–401
Erck A, Rainen L, Whileyman J, Chang IM, Kimball AP, Bear JL (1974) Studies of rhodium(II) carboxylates as potential antitumor agents. Proc Soc Exp Biol Med 145:1278–1283
Chifotides HT, Dunbar KR (2005) Interactions of metal−metal-bonded antitumor active complexes with DNA fragments and DNA. Acc Chem Res 38:146–156
Rubin JR, Haromy TP, Sundaralingam M (1991) Structure of the anti-cancer drug complex tetrakis(μ-acetato)-bis(1-methyl-adenosine)dirhodium(II) monohydrate. Acta Crystallogr C47:1712–1714
Aoki K, Salam MA (2002) Interligand interactions affecting specific metal bonding to nucleic acid bases. A case of Rh2(O2CCH3)4, Rh2(CF3CONH)4, and Rh2(O2CCH3)2(NHCOCF3)2 toward purine nucleobases and nucleosides. Inorg Chim Acta 339:427–437
Dunbar KR, Matonic JH, Saharan VP, Crawford CA, Christou G (1994) Structural evidence for a new metal-binding mode for guanine bases: implications for the binding of dinuclear antitumor agents to DNA. J Am Chem Soc 116:2201–2202
Crawford CA, Day EF, Saharan VP, Folting K, Huffman JC, Dunbar KR, Christou G (1996) N7,O6 bridging 9-ethylguanine (9-EtGH) groups in dinuclear metal-metal bonded complexes with bond orders of one, two or four. Chem Commun 1113–1114
Catalan KV, Mindiola DJ, Ward DL, Dunbar KR (1997) A novel dirhodium compound with neutral, bridging 9-ethyladenine ligands. Inorg Chem 36:2458–2460
Catalan KV, Hess JS, Maloney MM, Mindiola DJ, Ward DL, Dunbar KR (1999) Reactions of DNA purines with dirhodium formamidinate compounds that display antitumor behavior. Inorg Chem 38:3904–3913
Asara JM, Hess JS, Lozada E, Dunbar KR, Allison J (2000) Evidence for binding of dirhodium bis-acetate units to adjacent GG and AA sites on single-stranded DNA. J Am Chem Soc 122:8–13
Chifotides HT, Koomen JM, Kang M, Dunbar KR, Tichy S, Russell D (2004) Binding of DNA purine sites to dirhodium compounds probed by mass spectrometry. Inorg Chem 43:6177–6187
Tselepi-Kalouli E, Katsaros N (1990) The interaction of Rh(II) and Rh(III) with DNA. J Inorg Biochem 40:95–102
Pittet PA, Dadci L, Zbinden P, Abou-Hamdan A, Merbach AE (1993) High-pressure proton NMR study of acetonitrile exchange kinetics on [Rh2(CH3CN)10]4+ and 17O NMR investigation of aqueous solutions of [Rh2(H2O)10]4+. Inorg Chim Acta 206:135–140
Fu PK-L, Bradley PM, Turro C (2001) DNA cleavage by photogenerated Rh2(O2CCH3)4(H2O)2+. Inorg Chem 40:2476–2477
Bradley PM, Bursten BE, Turro C (2001) Excited-state properties of Rh2(O2CCH3)4(L)2 (L = CH3OH, THF, PPh3, py). Inorg Chem 40:1376–1379
Bradley PM, Angeles-Boza AM, Dunbar KR, Turro C (2004) Direct DNA photocleavage by a new intercalating dirhodium(II/II)complex: comparison to Rh2(μ-O2CCH3)4. Inorg Chem 43:2450–2452
Angeles-Boza AM, Bradley PM, Fu PK-L, Wicke SE, Bacsa J, Dunbar KR, Turro C (2004) DNA binding and photocleavage in vitro by new dirhodium(II) dppz complexes: correlation to cytotoxicity and photocytotoxicity. Inorg Chem 43:8510–8519
Angeles-Boza AM, Bradley PM, Fu PK-L, Shatruk M, Hilfiger MG, Dunbar KR, Turro C (2005) Photocytotoxicity of a new Rh2 (II, II) complex: increase in cytotoxicity upon irradiation similar to that of PDT agent hematoporphyrin. Inorg Chem 44:7262–7264
Lutterman DA, Fu PK-L, Turro C (2006) Cis-[Rh2(μ-O2CCH3)2(CH3CN)6]2+ as a photoactivated cisplatin analog. J Am Chem Soc 128:738–739
Li Z, Burya SJ, Turro C, Dunbar KR (2013) Photochemistry and DNA photocleavage by a new unsupported dirhodium(II, II) complex. Philos Trans R Soc A 371:20120128
Palmer AM, Burya SJ, Gallucci JC, Turro C (2014) Photoinduced intercalation and coordination of a dirhodium complex to DNA: dual DNA binding. ChemMedChem 9:1260–1265
Mahnken RE, Bina M, Deibel RM, Luebke K, Morrison H (1989) Photochemically induced binding of [Rh(phen)2Cl]2+ to DNA. Photochem Photobiol 49(4):519–522
Harmon HL, Momson H (1995) Anaerobic photoinduced N7-binding of cis-dichlorobis(1,10-phenanthroline)rhodium(III) chloride to 2′-deoxyguanosine process. Inorg Chem 34:4937–4938
Menon EL, Perera R, Navarro M, Kuhn RJ, Morrison H (2004) Phototoxicity against tumor cells and sindbis virus by an octahedral rhodium bisbipyridyl complex and evidence for the genome as a target in viral photoinactivation. Inorg Chem 43:5373–5381
Loganathan D, Morrison H (2006) Effect of ring methylation on the photophysical, photochemical and photobiological properties of cis-dichlorobis(1,10-phenanthroline)rhodium(III)chloride. Photochem Photobiol 82:237–247
Kim MR, Morrison H, Mohammeda SI (2011) Effect of a photoactivated rhodium complex in melanoma. Anticancer Drugs 2011(22):896–904
Magennis SW, Habtemariam A, Novakova O, Henry JB, Meier S, Parsons S, Oswald IDH, Brabec V, Sadler PJ (2007) Dual triggering of DNA binding and fluorescence via photoactivation of a dinuclear ruthenium(II) arene complex. Inorg Chem 46:5059–5068
Betanzos-Lara S, Salassa L, Habtemariam A, Sadler PJ (2009) Photocontrolled nucleobase binding to an organometallic RuII arene complex. Chem Commun 43:6622–6624
Betanzos-Lara S, Salassa L, Habtemariam A, Novakova O, Pizarro AM, Clarkson GJ, Liskova B, Brabec V, Sadler PJ (2012) Photoactivatable organometallic pyridyl ruthenium(II) arene complexes. Organometallics 31:3466–3479
Barragan F, Lopez-Senin P, Salassa L, Betanzos-Lara S, Habtemariam A, Moreno V, Sadler PJ, Marchan V (2011) Photocontrolled DNA binding of a receptor-targeted organometallic ruthenium(II) complex. J Am Chem Soc 133:14098–14108
Betanzos-Lara S, Habtemariam A, Sadler PJ (2013) Transfer hydrogenation reactions of photoactivatable N,N′-chelated ruthenium(II) arene complexes. J Mex Chem Soc 57:160–168
Lin S-J, Guarente L (2003) Nicotinamide adenine dinucleotide, a metabolic regulator of transcription, longevity and disease. Curr Opin Cell Biol 15:241–246
Romero-Canelón I, Sadler PJ (2013) Next-generation metal anticancer complexes: multitargeting via redox modulation. Inorg Chem 52:12276–12291
Watson J (2013) Perspective: oxidants, antioxidants and the current incurability of metastatic cancers. Open Biol 3:2046–2441
Sasmal PK, Carregal-Romero S, Parak WJ, Meggers E (2012) Light-triggered ruthenium-catalyzed allylcarbamate cleavage in biological environments. Organometallics 31:5968–5970
Singh TN, Turro C (2004) Photoinitiated DNA binding by cis- [Ru(bpy)2(NH3)2]2+. Inorg Chem 43:7260–7262
Sears RB, Joyce LE, Ojaimi M, Gallucci JC, Thummel RP, Turro C (2013) Photoinduced ligand exchange and DNA binding of cis-[Ru(phpy)(phen)(CH3CN)2]+ with long wavelength visible light. J Inorg Biochem 121:77–87
Palmer AM, Peña B, Sears RB, Chen O, Ojaimi ME, Thummel RP, Dunbar KR, Turro C (2013) Cytotoxicity of cyclometallated ruthenium complexes: the role of ligand exchange on the activity. Philos Trans R Soc 371:20120135
Wachter E, Heidary DK, Howerton BS, Parkin S, Glazer EC (2012) Light-activated ruthenium complexes photobind DNA and are cytotoxic in the photodynamic therapy window. Chem Commun 48:9649–9651
Howerton BS, Heidary DK, Glazer EC (2012) Strained ruthenium complexes are potent light-activated anticancer agents. J Am Chem Soc 134:8324–8327
Friedrich J, Seidel C, Ebner R, Kunz-Schughart LA (2009) Spheroid-based drug screen: considerations and practical approach. Nat Protoc 4(3):309–324
Sgambellone MA, David A, Garner RN, Dunbar KR, Turro C (2013) Cellular toxicity induced by the photorelease of a caged bioactive molecule: design of a potential dual-action Ru(II) complex. J Am Chem Soc 135:11274–11282
Joshi T, Pierroz V, Mari C, Gemperle L, Ferrari S, Gasser G (2014) A bis(dipyridophenazine)(2-(2-pyridyl)pyrimidine-4-carboxylic acid)ruthenium(II) complex with anticancer action upon photodeprotection. Angew Chem Int 126(11):3004–3007
Salassa L (2011) Polypyridyl metal complexes with biological activity. Eur J Inorg Chem 32:4931–4947
Barolet D (2008) Light-emitting diodes (LEDs) in dermatology. Semin Cutan Med Surg 27:227–238
Del Mármol J, Filevich O, Etchenique R (2010) A ruthenium−rhodamine complex as an activatable fluorescent probe. Anal Chem 82:6259–6264
Rose MJ, Betterley NM, Mascharak PK (2009) Thiolate S-oxygenation controls nitric oxide (NO) photolability of a synthetic iron nitrile hydratase (Fe-NHase) model derived from mixed carboxamide/thiolate ligand. J Am Chem Soc 131:8340–8341
Arguinzoniz AG, Ruggiero E, Habtemariam A, Hernández-Gil J, Salassa L, Mareque-Rivas JC (2014) Light harvesting and photoemission by nanoparticles for photodynamic therapy. Part Part Syst Charact 31:46–75
Maldonado CR, Salassa L, Gomez-Blanco N, Mareque-Rivas JC (2013) Nano-functionalization of metal complexes for molecular imaging and anticancer therapy. Coord Chem Rev 257:2668–2688
Burks PT, Ostrowski AD, Mikhailovsky AA, Chan EM, Wagenknecht PS, Ford PC (2012) Quantum dot photoluminescence quenching by Cr(III) complexes. Photosensitized reactions and evidence for a FRET mechanism. J Am Chem Soc 134:13266–13275
Neuman D, Ostrowski AD, Mikhailovsky AA, Absalonson RO, Strouse GF, Ford PC (2008) Quantum dot fluorescence quenching pathways with Cr(III) complexes. Photosensitized NO production from trans-Cr(cyclam)(ONO)2+. J Am Chem Soc 130:168–175
Blanco NG, Maldonado CR, Mareque-Rivas JC (2009) Effective photoreduction of a Pt(IV) complex with quantum dots: a feasible new light-induced method of releasing anticancer Pt(II) drugs. Chem Commun 35:5257–5259
Hernández-Gil J, Llusar SF, Maldonado CR, Mareque-Rivas JC (2011) Synergy between quantum dots and 1,10-phenanthroline–copper(II) complex towards cleaving DNA. Chem Commun 47:2955–2957
Infante I, Azpiroz JM, Blanco NG, Ruggiero E, Ugalde JM, Mareque-Rivas JC, Salassa L (2014) Quantum dot photoactivation of Pt(IV) anticancer agents: evidence of an electron transfer mechanism driven by electronic coupling. J Phys Chem C 118:8712–8721
Maldonado CR, Gómez-Blanco N, Jauregui-Osoro M, Brunton VG, Yate L, Mareque-Rivas JC (2013) QD-filled micelles which combine SPECT and optical imaging with light-induced activation of a platinum(IV) prodrug for anticancer applications. Chem Commun 49:3985–3987
Zhou J, Liu Z, Li F (2012) Upconversion nanophosphors for small-animal imaging. Chem Soc Rev 41:1323–1349
Burks PT, Garcia JV, Gonzalez Irias R, Tillman JT, Niu M, Mikhailovsky AA, Zhang J, Zhang F, Ford PC (2013) Nitric oxide releasing materials triggered by near-infrared excitation through tissue filters. J Am Chem Soc 135:18145–18152
Garcia JV, Yang J, Shen D, Yao C, Li X, Wang R, Stucky GD, Zhao D, Ford PC, Zhang F (2012) NIR-triggered release of caged nitric oxide using upconverting nanostructured materials. Small 8:3800–3805
Ruggiero E, Habtemariam A, Yate L, Mareque-Rivas JC, Salassa L (2014) Near infrared photolysis of a Ru polypyridyl complex by upconverting nanoparticles. Chem Commun 50:1715–1718
Frasconi M, Liu Z, Lei J, Wu Y, Strekalova E, Malin D, Ambrogio MW, Chen X, Botros YY, Cryns VL, Sauvage J-P, Stoddart JF (2013) Photoexpulsion of surface-grafted ruthenium complexes and subsequent release of cytotoxic cargos to cancer cells from mesoporous silica nanoparticles. J Am Chem Soc 135:11603–11613
Acknowledgments
This work was supported by Spanish Ministry of Economy and Competitiveness (grant CTQ2012-39315), the Department of Industry of the Basque Country (grant ETORTEK), the MICINN of Spain with the Ramón y Cajal Fellowship RYC-2011-07787, and by the MC CIG fellowship UCnanomat4iPACT (grant n. 321791). S.A. thanks the Spanish Ministry of Economy and Competitiveness for funding her PhD fellowship (BES-2013-065642). We gratefully acknowledge IKERBASQUE for the Visiting Professor Fellowship to A.H. and members of the European COST Action CM1105 for stimulating discussions.
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Ruggiero, E., Alonso-de Castro, S., Habtemariam, A., Salassa, L. (2014). The Photochemistry of Transition Metal Complexes and Its Application in Biology and Medicine. In: Lo, KW. (eds) Luminescent and Photoactive Transition Metal Complexes as Biomolecular Probes and Cellular Reagents. Structure and Bonding, vol 165. Springer, Berlin, Heidelberg. https://doi.org/10.1007/430_2014_165
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