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Structure and conformation of photosynthetic pigments and related compounds. 15. Conformational analysis of chlorophyll derivatives - implications for hydroporphyrins in vivo

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Abstract

Chlorophylls are fundamental macrocyclic cofactors in photosynthetic reaction centers and light-harvesting complexes. Their biological function is well understood on the basis of protein structural data and a significant body of information indicates that the conformation of tetrapyrroles plays a large role in controlling their biological activity. While there is no small molecule crystal structure of chlorophyll, the normal-coordinate structural decomposition (NSD) method is a very useful analytical tool for conformational analysis of chlorophylls, using tetrapyrroles that mimic their structure. NSD allows for an analysis of the individual macrocyclic distortion modes and their contributions to the overall conformation. Herein, we present our own validation of the NSD program and use it to carry out a conformational analysis of chlorophyll-related compounds. Metal insertions, peripheral substi-tuents, and solvents in the unit cell give rise to different NSD profiles in chlorophyll derivatives. These range from planar and non-planar conformations upon metal insertions, to polar peripheral substituents, and fused rings in chlorins. Substituent effects are clearly evidenced in highly β-substituted chlorins and while bacteriochlorins and isobacteriochlorins experience similar effects to the chlorins, they are also subject to solvent effects, causing the macrocycle to be non-planar. Overall, we report a first conformational analysis of all 'chlorophyll'-related small molecule crystal structures at an atomic level.

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References

  1. M. O. Senge, A. A. Ryan, K. A. Letchford, S. A. MacGowan and T. Mielke, Chlorophylls. Symmetry, chirality and photosynthesis, Symmetry, 2014, 6, 781–843.

    Article  Google Scholar 

  2. H. Scheer, Chlorophylls, CRC Press, Boca Raton, 1991.

    Google Scholar 

  3. A. A. Ryan and M. O. Senge, How green is green chemistry? Chlorophylls as a bioresource from biorefineries and their commercial potential in medicine and photovoltaics, Photochem. Photobiol. Sci., 2015, 14, 638–660.

    Article  CAS  PubMed  Google Scholar 

  4. J. Deisenhofer, O. Epp, K. Miki, R. Huber and H. Michel, Structure of the protein subunits in the photosynthetic reacton centre of Rhodopseudomonas viridus at 3 Â resolution, Nature, 1985, 318, 618–624

    Article  CAS  PubMed  Google Scholar 

  5. G. McDermott, S. M. Prince, A. A. Freer, A. M. Hawthornewaite-Lawless, M. Z. Papiz, R. J. Cogdell and N. W. Isaacs, Crystal Structure of an integral membrane light-harvesting complex from photosynthetic bacteria, Nature, 1995, 374, 517–521

    Article  CAS  Google Scholar 

  6. P. Jordan, P. Fromme, H. T. Witt, O. Klukas, W. Saenger and N. Krauss, Structure of photosystem I, Nature, 2001, 411, 909–917.

    Article  CAS  PubMed  Google Scholar 

  7. A. Forman, M. W. Renner, E. Fujita, K. M. Barkigia, M. C. W. Evans, K. M. Smith and J. Fajer, ESR and ENDOR Probes of skeletal conformations implications for conformations and orientations of chlorophylls in vivo, Isr. J. Chem., 1989, 29, 57–64

    Article  CAS  Google Scholar 

  8. M. O. Senge, New trends in photobiology. The conformational flexibility of tetrapyrroles - Current model studies and photobiological implications, J. Photochem. Photobiol., B, 1992, 16, 3–36.

    Article  CAS  Google Scholar 

  9. E. B. Fleischer, Structure of porphyrins and metallopor- phyrins, Acc. Chem. Res., 1970, 3, 105–112

    Article  CAS  Google Scholar 

  10. C. J. Medforth, M. O. Senge, K. M. Smith, L. D. Sparks and J. A. Shelnutt, Nonplanar distortion modes for highly substituted porphyrins, J. Am. Chem. Soc., 1992, 114, 9859–9869

    Article  CAS  Google Scholar 

  11. M. O. Senge, in The Porphyrin Handbook, ed. K.M. Kadish, K.M. Smith and R. Guilard, Academic Press, San Diego, 2000, vol. 1, pp. 239–347.

    Google Scholar 

  12. M. O. Senge, Exercises in molecular gymnastics—Bending, stretching and twisting porphyrins, Chem. Commun., 2006, 243–256.

    Google Scholar 

  13. E. Gudowska-Nowak, M. D. Newton and J. Fajer, Conformational and environmental effects on bacteriochlorophyll optical spectra: correlations of calculated spectra with structural results, J. Phys. Chem., 1990, 94, 5795–5801.

    Article  CAS  Google Scholar 

  14. M. O. Senge, S. A. MacGowan and J. M. O'Brien, Conformational control of cofactors in nature - the influence of protein-induced macrocycle distortion on the biological function of tetrapyrroles, Chem. Commun., 2015, 51, 17031–17063.

    Article  CAS  Google Scholar 

  15. W. Jentzen, J. G. Ma and J. A. Shelnutt, Conservation of the conformation of the porphyrin macrocycle in hemoproteins, Biophys. J., 1998, 74, 753–763.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. S. A. MacGowan and M. O. Senge, Conformational control of cofactors in nature functional tetrapyrrole conformations in the photosynthetic reaction centers of purple bacteria, Chem. Commun., 2011, 47, 11621–11623.

    Article  CAS  Google Scholar 

  17. D. Bednarczyk, O. Dym, V. Prabahar, Y. Peleg, D. H. Pike and D. Noy, Fine tuning of chlorophyll spectra by protein-induced ring deformation, Angew. Chem., Int. Ed., 2016, 55, 6901–6905.

    Article  CAS  Google Scholar 

  18. C. Kratky, R. Waditschatka, J. E. Johansen, J. C. Plaquevent, J. Schreiber and A. Eschenmoser, Die sattelkonformation der hydroporphinoiden nickel(II)-komplexe: Struktur, ursprung und stereochemische consequenzen, Helv. Chim. Acta, 1985, 68, 1312–1337.

    Article  CAS  Google Scholar 

  19. M. O. Senge and S. A. MacGowan, in Handbook of Porphyrin Science, ed. K.M. Kadish, K.M. Smith and R. Guilard, World Scientific, Singapore, 2010, vol. 13, pp. 253–297.

    Google Scholar 

  20. K. M. Barkigia, L. Chantranupong, K. M. Smith and J. Fajer, Structural and theoretical models of photosynthetic chromophores. Implications for redox, light-absorption properties and vectoral electron flow, J. Am. Chem. Soc., 1988, 110, 7566–7567.

    Article  CAS  Google Scholar 

  21. M. O. Senge and K. M. Smith, Structure and conformation of photosynthetic pigments and related compounds. 2. Nickel(II) methyl pyropheophorbide a- A severely distorted chlorophyll derivative, Photochem. Photobiol., 1991, 54, 841–846.

    Article  CAS  Google Scholar 

  22. A. M. Stolzenberg and M. T. Stershic, Reductive chemistry of nickel hydroporphyrins. evidence for a biologically significant difference between porphyrins, hydroporphyrins, and other tetrapyrroles, J. Am. Chem. Soc., 1988, 110, 6391–6402

    Article  CAS  Google Scholar 

  23. A. M. Stolzenberg, L. J. Schussel, J. S. Summers, B. M. Foxman and J. L. Petersen, Structures of the homologoues series of square-planar metallotetrapyrroles palladium(II) octaethylporphyrin, palladium(II) trans-octaethylchlorin, and palladium(II) tct-octaethyl-isobacteriochlorin, Inorg. Chem., 1992, 31, 1678–1686.

    Article  CAS  Google Scholar 

  24. For a detailed description of all cases see ref. 5, 9 and 14.

  25. W. Jentzen, X. Z. Song and J. A. Shelnutt, Structural characterization of synthetic and protein-bound porphyrins in terms of the lowest-frequency normal coordinates of the macrocycle, J. Phys. Chem. B, 1997, 101, 1684–1699.

    Article  CAS  Google Scholar 

  26. C. R. Groom, I. J. Bruno, M. P. Lightfoot and S. C. Ward, The Cambridge Structural Database, Acta Crystallogr., Sect. B: Struct. Sci., Cryst. Eng. Mater., 2016, 72, 171–179.

    Article  CAS  Google Scholar 

  27. I. J. Bruno, J. C. Cole, P. R. Edgington, M. Kessler, C. F. Macrae, P. McCabe, J. Pearson and R. Taylor, New software for searching the Cambridge Structural Database and visualizing crystal structures, Acta Crystallogr., Sect. B: Struct. Sci., Cryst. Eng. Mater., 2002, 58, 389–397.

    Article  CAS  Google Scholar 

  28. C. F. Macrae, I. J. Bruno, J. A. Chisholm, P. R. Edgington, P. McCabe, E. Pidcock, L. Rodriguez-Monge, R. Taylor, J. van de Streek and P. A. Wood, Mercury CSD 2.0 - New features for the visualization and investigation of crystal structures, J. Appl. Crystallogr., 2008, 41, 466–470.

    Article  CAS  Google Scholar 

  29. S. A. MacGowan and M. O. Senge, Contribution of bacteriochlorophyll conformation to the distribution of site-energies in the FMO protein, Biochim. Biophys. Acta, Bioenerg., 2016, 1857, 427–442.

    Article  CAS  Google Scholar 

  30. L. Sun and J. A. Shelnutt, NSDGUI (Version 1.3 Alpha version), Sandia National Laboratory, Albuquerque, USA, 2000-2001.

    Google Scholar 

  31. M. P. Byrn, C. J. Curtis, I. Goldberg, Y. Hsiou, S. I. Khan, P. A. Sawin, S. K. Tendick and C. E. Strouse, Porphyrin sponges: structural systematics of the host lattices, J. Am. Chem. Soc., 1991, 113, 6549–6557

    Article  CAS  Google Scholar 

  32. M. P. Byrn, C. J. Curtis, S. I. Khan, P. A. Sawin and C. E. Strouse, Tetraarylporphyrin sponges. Composition, structural systematics, and applications of a large class of programmable lattice clathrates, J. Am. Chem. Soc., 1990, 112, 1865–1874

    Article  CAS  Google Scholar 

  33. G. L. Perlovich, W. Zielenkiewicz, Z. Kaszkur and J. Slowikowska, The thermochemistry of polymorphs and crystalline solvates based on tetraphenylporphyrins and its zinc complex, J. Mol. Liq., 2002, 95, 243–259

    Article  CAS  Google Scholar 

  34. S. J. Silver and A. Tulinsky, The crystal and molecular structure of triclinic tetraphenylporphyrin, J. Am. Chem. Soc., 1967, 89, 3331–3337

    Article  Google Scholar 

  35. G. Donnay and C. B. Storm, Molecular solid solution of tetraphenyl-porphyrin and silver tetraphenylporphyrin, Mol. Cryst., 1967, 2, 287–292

    Article  CAS  Google Scholar 

  36. K. Kano, K. Fukuda, H. Wakami, R. Nishiyabu and R. F. Pasternack, Factors influencing self-aggregation tendencies of cationic porphyrins in aqueous solution, J. Am. Chem. Soc., 2000, 122, 7494–7502

    Article  CAS  Google Scholar 

  37. B. L. Barker, G. G. Stanley and F. R. Fronczek, CSD Commun., 2002, CCDC 188202

    Google Scholar 

  38. C. Brückner, J. Ogikubo, J. R. McCarthy, J. Akhigbe, M. A. Hyland, P. Daddario, J. L. Worlinsky, M. Zeller, J. T. Engle, C. J. Ziegler, M. J. Ranaghan, M. N. Sandberg and R. R. Birge, Meso-Arylporpholactones and their reduction products, J. Org. Chem., 2012, 77, 6480–6494

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  39. M. E. Light, T. Bandy and E. Stulz, CSD Commun., 2016, CCDC 1476315

    Google Scholar 

  40. Z. Li, Y. Hu and T. Li, Crystal structure and third-order nonlinear optical properties study of tetraphenylporphyrin and its nickel complex at wavelength 532 nm and 1064 nm, Mol. Cryst. Liq. Cryst., 2014, 605, 135–145

    Article  CAS  Google Scholar 

  41. J. Blömker and W. Frey, Crystal structure of anthracene—5,10,15,20-tetraphenyl-21H,23H-porphyrin (1/ 1), C58H40N4, Z. Kristallogr. - New Cryst. Struct., 2000, 215, 267–268

    Article  Google Scholar 

  42. J. Blömker and W. Frey, Crystal structure of pyrene—5,10,15,20-tetraphenyl-21H,23H-porphyrin (1/1), C60H40N4, Z. Kristallogr. - New Cryst. Struct., 2000, 215, 263–264.

    Article  Google Scholar 

  43. J. W. Lauher and J. A. Ibers, Structure of octaethylporphyrin. Comparison with other free base porphyrins, J. Am. Chem. Soc., 1973, 95, 5148–5152

    Article  CAS  PubMed  Google Scholar 

  44. M. M. Olmstead, A. de Bettencourt-Dias, H. M. Lee, D. Pham and A. L. Balch, Interactions of metalloporphyrins as donors with the electron acceptors C60, tetracyanoquindimethane (TCNQ) and trinitrofluorenylidenemalonitrile, Dalton Trans., 2003, 3227–3232.

    Google Scholar 

  45. W. W. Kalisch and M. O. Senge, Synthesis and structural characterization of nonplanar tetraphenylporphyrins with graded degree of ß-ethyl substitution, Tetrahedron Lett., 1996, 37, 1183–1186

    Article  CAS  Google Scholar 

  46. M. O. Senge and W. W. Kalisch, Synthesis and structural characterization of nonplanar tetraphenylporphyrins and their metal complexes with graded degrees of ß-ethyl substitution, Inorg. Chem., 1997, 36, 6103–6116

    Article  CAS  PubMed  Google Scholar 

  47. Y. Yamamoto, A. Yamamoto, S. Furuta, M. Horie, M. Kodama, W. Sato, K. Akiba, S. Tsuzuki, T. Uchimara, D. Hasizume and F. Iwasaki, Synthesis and structure of 16 n octaalkyltetraphenylporphyrins, J. Am. Chem. Soc., 2005, 127, 14540–14541.

    Article  CAS  PubMed  Google Scholar 

  48. M. O. Senge, W. W. Kalisch and S. Runge, Conformationally distorted chlorins via diimide reduction of nonplanar porphyrins, Tetrahedron, 1998, 54, 3781–3798.

    Article  CAS  Google Scholar 

  49. W. Jentzen, M. C. Simpson, J. D. Hobbs, X. Song, T. Ema, N. Y. Nelson, C. J. Medforth, K. M. Smith, M. Veyrat, M. Mazzanti, R. Ramasseul, J.-C. Marchon, T. Takeuchi, W. A. Goddard III and J. A. Shelnutt, Ruffling in a series of nickel(II) meso-tetrasubstituted porphyrins as a model for the conserved ruffling of the heme of cytochromes c, J. Am. Chem. Soc., 1995, 117, 11085–11097.

    Article  CAS  PubMed  Google Scholar 

  50. W. R. Scheidt, J. U. Mondal, C. W. Eigenbrot, A. Adler, L. J. Radonovich and J. L. Hoard, Crystal and molecular structure of the silver(II) and zinc(II) derivatives of mesotetraphenylporphyrin. An exploration of crystal-packing effects on bond distance, Inorg. Chem., 1986, 25, 795–799.

    Article  CAS  Google Scholar 

  51. A. Ozarowski, H. M. Lee and A. L. Balch, Crystal environments probed by epr spectroscopy. variations in the EPR spectra of CoII(octaethylporphyrin) doped in crystalline diamagnetic hosts and a reassessment of the electronic structure of four-coordinate cobalt (II), J. Am. Chem. Soc., 2003, 125, 12606–12614

    Article  CAS  PubMed  Google Scholar 

  52. K. M. Barkigia, M. D. Berber, J. Fajer, C. J. Medforth, M. W. Renner and K. M. Smith, Nonplanar porphyrins. X-ray structures of (2,3,7,8,12,13,17,18-octaethyl- and -octamethyl-5,10,15,20-tetraphenylporphyri-nato)zinc(II), J. Am. Chem. Soc., 1990, 112, 8851–8857.

    Article  CAS  Google Scholar 

  53. M. P. Byrn, C. J. Curtis, Y. Hsiou, S. I. Khan, P. A. Sawin, S. K. Tendick, A. Terzis and C. E. Strouse, Porphyrin sponges: conservative of host structure in over 200 porphyrin-based lattice clathrates, J. Am. Chem. Soc., 1993, 115, 9480–9497.

    Article  CAS  Google Scholar 

  54. M. S. Fischer, D. H. Templeton, A. Zalkin and M. Calvin, Crystal and molecular structure of methyl pheo- phorbide with applications to the chlorophyll arrangement in photosynthetic lamellae, J. Am. Chem. Soc., 1972, 94, 3613–3619

    Article  CAS  Google Scholar 

  55. K. Takahashi, M. Obayashi and Y. Nishikawa, Kinki Daigaku Rikogakubu Kenkyu Hokoku, 1984, 85–92

    Google Scholar 

  56. L. Kutschabsky and G. Reck, CSD Commun., 2003, CCDC 215718

    Google Scholar 

  57. C. F. Chee, N. A. Rahman, S. M. Zain and S. W. Ng, Pheophorbide b ethyl ester from a Chlorella vulgaris dietary supplement, Acta Crystallogr., Sect. E: Struct. Rep. Online, 2008, 64, o1986–o1987

    Article  CAS  Google Scholar 

  58. K. M. Smith, D. A. Goff, J. Fajer and K. M. Barkigia, Chirality and structures of bacteriochlorophylls d, J. Am. Chem. Soc., 1982, 104, 3747–3749

    Article  CAS  Google Scholar 

  59. M. O. Senge, F. W. Bobe, M. S. Huster and K. M. Smith, Preparation and crystal structure of methyl [12-acetyl-8-ethyl]-bacteriopheophorbide d - A new bacteriochlorophyll derivative, Liebigs Ann., 1991, 871–874

    Google Scholar 

  60. K. M. Smith, D. A. Goff, J. Fajer and K. M. Barkigia, Isolation and characterization of two new bacteriochlorophylls d bearing neopentyl substituents, J. Am. Chem. Soc., 1983, 105, 1674–1676.

    Article  CAS  Google Scholar 

  61. M. O. Senge and K. M. Smith, Structure and confor mation of photosynthetic pigments and related compounds. 10. Comparison of a phytochlorin and phytoporphyrin derived from chlorophyll a, Acta Crystallogr., Sect. C: Cryst. Struct. Commun., 1997, 53, 1314–1318

    Article  Google Scholar 

  62. M. O. Senge and K. M. Smith, Structure and conformation of photosynthetic pigments and related compounds. 1. Methyl mesopyropheophorbide a, Z. Kristallogr., 1992, 199, 239–248

    Article  CAS  Google Scholar 

  63. Y. Kinoshita, M. Kunieda, Y. Mikata and H. Tamiaki, Synthesis, crystal structure, and electronic absorption of chlorophyll derivatives possessing a ß-diketonate moiety at the C3 position, Tetrahedron Lett., 2013, 54, 1243–1246.

    Article  CAS  Google Scholar 

  64. C. Kratky, H. P. Isenring and J. D. Dunitz, Methylpyrochlorophyllide a monohydrate monoetherate, Acta Crystallogr., Sect. B: Struct. Sci., Cryst. Eng. Mater., 1977, 33, 547–549

    Article  Google Scholar 

  65. C. Kratky and J. D. Dunitz, Methylchlorophyllide a dihydrate, Acta Crystallogr., Sect. B: Struct. Sci., Cryst. Eng. Mater., 1977, 33, 545–547

    Article  Google Scholar 

  66. C. Kratky and J. D. Dunitz, Comparison of the results of two independent analyses of the ethylchlorophyllide a dihydrate crystal structure, Acta Crystallogr., Sect. B: Struct. Sci., Cryst. Eng. Mater., 1975, 31, 1586–1589

    Article  Google Scholar 

  67. R. Serlin, H.-C. Chow and C. E. Strouse, Crystal and molecular structure of ethyl chlorophyllide b dihydrate at -153°, J. Am. Chem. Soc., 1975, 97, 7237–7242

    Article  CAS  Google Scholar 

  68. H.-C. Chow, R. Serlin and C. E. Strouse, Crystal and molecular structure and absolute configuration of ethyl chlorophyllide a dihydrate. A model for the different spectral forms of chlorophyll a, J. Am. Chem. Soc., 1975, 97, 7230–7237.

    Article  CAS  Google Scholar 

  69. S. Knapp, B. Huang, T. J. Emge, S. Sheng, K. Krogh-Jespersen, J. A. Potenza and H. J. Schuga, A pyropheophor-bide dimer with single pyrrole n overlap and a low-energy Q absorption, J. Am. Chem. Soc., 1999, 121, 7977–7978

    Article  CAS  Google Scholar 

  70. A. Jesorka, A. R. Holzwarth, A. Eichhofer, C. M. Reddy, Y. Kinoshita, H. Tamiaki, M. Katterle, J.-V. Naubron and T. S. Balaban, Water coordinated zinc dioxo-chlorin and porphyrin self-assemblies as chlorosomal mimics: variability of supramolecular interactions, Photochem. Photobiol. Sci., 2012, 11, 1069–1080

    Article  CAS  PubMed  Google Scholar 

  71. Y. Shinozaki, I. Yoshikawa, K. Araki, K. Sugawa and J. Otsuki, Control of higher-order structures of zinc chlorophyll coordination polymers, CrystEngComm, 2014, 16, 9155–9157

    Article  CAS  Google Scholar 

  72. Y. Shinozaki, G. Richards, K. Ogawa, A. Yamano, K. Ohara, K. Yamaguchi, S. Kawano, K. Tanaka, Y. Araki, T. Wada and J. Otsuki, Double helices of a pyridine-appended zinc chlorophyll derivative, J. Am. Chem. Soc., 2013, 135, 5262–5265

    Article  CAS  PubMed  Google Scholar 

  73. Y. Shinozaki, I. Yoshikawa, K. Araki, K. Ohara, K. Yamaguchi, S. Kawano, K. Tanaka, Y. Araki, T. Wada and J. Otsuki, Coordination oligomers and polymers of an oxazole-appended zinc chlorophyll derivative, Chem. Lett., 2014, 43, 862–864.

    Article  CAS  Google Scholar 

  74. M. O. Senge and K. M. Smith, Structure and conformation of photosynthetic pigments and related compounds. 7. on the conformation of the methyl ester of (20-methyl-phyto-chlorinato)nickel(II) - A bacteriochlorophyll c model compound, Photochem. Photobiol., 1994, 60, 139–142.

    Article  CAS  PubMed  Google Scholar 

  75. I. de Boer, J. Matysik, M. Amakawa, S. Yagai, H. Tamiaki, A. R. Holzwarth and H. J. M. de Groot, MAS NMR structure of a microcrystalline Cd-bacteriochlorophyll d analogue, J. Am. Chem. Soc., 2003, 125, 13374–13375

    Article  PubMed  CAS  Google Scholar 

  76. I. A. Zamilatskov, E. V. Savinkina, A. N. Volov, M. S. Grigorev, I. S. Lonin, L. N. Obolenskaya, G. V. Ponomarev, O. I. Koifman, A. S. Kuzovlev, G. M. Kuzmicheva and A. Y. Tsivadze, Syntheses, structures and photosensitizing properties of new Pt(II), Macroheterocycles, 2012, 5, 308–314

    Article  Google Scholar 

  77. M. O. Senge, K. Ruhlandt-Senge and K. M. Smith, Structure and conformation of photosynthetic pigments and related compounds, 8. molecular structure of an iron(III) chlorophyll derivative - Chloro( phytochlorinato methyl ester)iron(III), Z. Naturforsch., B: Chem. Sci., 1995, 50, 139–146.

    Article  CAS  Google Scholar 

  78. A. N. Kozyrev, V. Suresh, S. Das, M. O. Senge, M. Shibata, T. J. Dougherty and R. K. Pandey, Synthesis and spectroscopic studies of novel chlorins with fused quinoxaline or benzimidazole ring systems and related dimers with extended conjugation, Tetrahedron, 2000, 56, 3353–3447.

    Article  CAS  Google Scholar 

  79. K. M. Barkigia and D. S. Gottfried, A new crystal form of methyl bacteriopheophorbide a, Acta Crystallogr., Sect. C: Cryst. Struct. Commun., 1994, 50, 2069–2072

    Article  Google Scholar 

  80. K. M. Barkigia, D. S. Gottfried, S. G. Boxer and J. Fajer, A high-precision structure of a bacteriochlorophyll derivative, methyl bacteriopheophorbide a, J. Am. Chem. Soc., 1989, 111, 6444–6446

    Article  CAS  Google Scholar 

  81. K. M. Barkigia, J. Fajer, K. M. Smith and G. J. B. Williams, Crystal and molecular structure of methyl bacteriopheophorbide a. A model for a primary electron acceptor in bacterial photosynthesis, J. Am. Chem. Soc., 1981, 103, 5890–5893.

    Article  CAS  Google Scholar 

  82. M. Ptaszek, B. E. McDowell, M. Taniguchi, H. J. Kim and J. S. Lindsey, Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. Part 1: Synthesis, Tetrahedron, 2007, 63, 3826–3839

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. J. S. Lindsey, De novo, synthesis of gem-dialkyl chlorophyll analogues for probing and emulating our green world, Chem. Rev., 2015, 115, 6534–6620

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. M. Taniguchi and J. S. Lindsey, Synthetic chlorins, possible surrogates for chlorophylls, prepared by derivatization of porphyrins, Chem. Rev., 2017, 117, 344–535.

    Article  CAS  PubMed  Google Scholar 

  85. M. Taniguchi, O. Mass, P. D. Boyle, Q. Tang, J. R. Diers, D. F. Bocian, D. Holten and J. S. Lindsey, Structural studies of sparsely substituted synthetic chlorins and phorbines establish benchmarks for changes in the ligand core and framework of chlorin macrocycles, J. Mol. Struct., 2010, 979, 27–45

    Article  CAS  Google Scholar 

  86. O. Mass, M. Ptaszek, M. Taniguchi, J. R. Diers, H. L. Kee, D. F. Bocian, D. Holten and J. S. Lindsey, Synthesis and photochemical properties of 12-substitued versus 13-substituted chlorins, J. Org. Chem., 2009, 74, 5276–5289

    Article  CAS  PubMed  Google Scholar 

  87. R. Xiong, A. I. Arkhypchuk, D. Kovacs, A. Orthaber and K. E. Borbas, Directly linked hydroporphyrin dimers, Chem. Commun., 2016, 52, 9056–9058

    Article  CAS  Google Scholar 

  88. R. Li, M. Zeller, T. Bruhn and C. Brückner, Surprising outcomes of classic ring-expansion conditions applied to octaethyloxochlorin, 3. Schmidt-reaction conditions, Eur. J. Org. Chem., 2017, 1835–1842

    Google Scholar 

  89. R. Li, E. Meehan, M. Zeller and C. Brückner, Surprising outcomes of classic ring-expansion conditions applied to octaethyloxochlorin, 2. Beckmann rearrangement conditions, Eur. J. Org. Chem., 2017, 1826–1834

    Google Scholar 

  90. R. Li, M. Zeller and C. Brückner, Surprising outcomes of classic ring-expansion conditions applied to octaethyloxochlorin, 1. Baeyer-Villager oxidation conditions, Eur. J. Org. Chem., 2017, 1820–1825

    Google Scholar 

  91. K. M. Barkigia, C. K. Chang and J. Fajer, Molecular structure of a dihydroxychlorin. A model of the green heme d and of a photodynamic therapy sensitizer, J. Am. Chem. Soc., 1991, 113, 7445–7447

    Article  CAS  Google Scholar 

  92. W. Hoppe, G. Will, J. Gassmann and H. Weichselgartner, Die kristall-und molekülstruktur von phyllochlorinester, Z. Kristallogr., 1969, 128, 18–31

    Article  Google Scholar 

  93. K. M. Shea, L. Jaquinod, R. G. Khoury and K. M. Smith, Dodecasubstituted metallochlorins (metallodihydroporphyrins), Chem. Commun., 1998, 759–760

    Google Scholar 

  94. M. O. Senge, W. W. Kalisch and I. Bischoff, The reaction of porphyrins with organolithium reagents, Chem. - Eur. J., 2000, 6, 2721–2738

    Article  CAS  PubMed  Google Scholar 

  95. J. L. Worlinsky, G. Zarate, M. Zeller, M. Ghandehari, G. Khalil and C. Brückner, Oxazolochlorins 11: Tuning the dynamic high pH sensing range of [meso-tetraarylporpholactonato]M(II) complexes by variation of the central metal ion, the aryl substituents, and the introduction of a ß-nitro group, J. Porphyrins Phthalocyanines, 2013, 17, 836–849.

    Article  CAS  Google Scholar 

  96. M. Taniguchi, M. Ptaszek, B. E. McDowell, P. D. Boyle and J. S. Lindsey, Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. Part 3: Spectral and structural properties, Tetrahedron, 2007, 63, 3850–3863

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  97. C. Muthiah, M. Ptaszek, T. M. Nguyen, K. M. Flack and J. S. Lindsey, Two complementary routes to 7-substituted chlorins. partial mimics of chlorophyll b, J. Org. Chem., 2007, 72, 7736–7749

    Article  CAS  PubMed  Google Scholar 

  98. W. R. Scheidt, H. F. Duval, T. J. Neal and M. K. Ellison, Intrinsic structural distortions in five-coordinate (nitrosyl)iron(II) poprhyrinate derivatives, J. Am. Chem. Soc., 2000, 122, 4651–4659

    Article  CAS  Google Scholar 

  99. P. A. Connick, K. J. Haller and K. A. Macor, X-ray structural and imidazole-binding studies of nickel ß-oxoporphyrins, Inorg. Chem., 1993, 32, 3256–3264

    Article  CAS  Google Scholar 

  100. S. Cai, E. Belikova, L. A. Yatsunyk, A. M. Stolzenberg and F. A. Walker, Magnetic resonance and structural investigations of (monooxooctaethylchlorinato)iron(III) chloride and its bis(imidazole) complex, Inorg. Chem., 2005, 44, 1882–1889

    Article  CAS  PubMed  Google Scholar 

  101. A. M. Stolzenberg, P. A. Glazer and B. M. Foxman, Structure, Reactivity, and electrochemistry of free base ß-oxoporphyrins and metallo-ß-oxoporphyrins, Inorg. Chem., 1986, 25, 983–991

    Article  CAS  Google Scholar 

  102. K. M. Barkigia, M. A. Thompson, J. Fajer, R. K. Pandey, K. M. Smith and M. G. H. Vicente, Conformational flexibility of chlorin macrocycles. Structural determinations and theoretical calculations of benzochlorin, a meso-dimethyl chlorin and a nickel chlorin, New J. Chem., 1992, 16, 599–607.

    CAS  Google Scholar 

  103. F.-P. Montforts, A. Meier, G. Scheurich, G. Haake and J. W. Bats, Chlorins designed for photodynamic tumor therapy and as model systems for photosynthesis, Angew. Chem., Int. Ed. Engl., 1992, 31, 1592–1594

    Article  Google Scholar 

  104. J. J. Lin, K. R. Gerzevske, P. A. Liddell, M. O. Senge, M. M. Olmstead, R. G. Khouiy, B. E. Weeth, S. A. Tsao and K. M. Smith, Metal-catalyzed oxidative cyclizations of a,c-biladiene salts bearing 1-and/or 19- arylmethyl substituents: macrocyclic products and their chemistry, J. Org. Chem., 1997, 62, 4266–4276

    Article  CAS  PubMed  Google Scholar 

  105. P. A. Liddell, K. R. Gerzevske, J. J. Lin, M. M. Olmstead and K. M. Smith, Novel macrocycles from metal-catalyzed oxidative cyclizations of a,c-biladiene salts, J. Org. Chem., 1993, 58, 6681–6691

    Article  CAS  Google Scholar 

  106. W. W. Kalisch, M. O. Senge and K. Ruhlandt-Senge, Synthesis and structural characterization of cofacial bisoctaethylchlorins as models for the special pair, Photochem. Photobiol., 1998, 67, 312–323

    Article  CAS  Google Scholar 

  107. N. Chaudhri, N. Grover and M. Sankar, Versatile synthetic route for ß-functionalized chlorins and porphyrins by varying the size of Michael donors: Syntheses, photophysical, and electrochemical redox properties, Inorg. Chem., 2017, 56, 11532–11545

    Article  CAS  PubMed  Google Scholar 

  108. S. Banerjee, M. Zeller and C. Brückner, Meso-Tetraphenylporphryin-derived oxypyriporphyrin, oxypyrichlorin, and thiomorpholinochlorin, as their Ni(II) complexes, J. Porphyrins Phthalocyanines, 2012, 16, 576–588.

    Article  CAS  Google Scholar 

  109. E. Skrzypczak-Jankun, CSD Commun. (Private Communication), 2000, CDC 144165

    Google Scholar 

  110. D. P. Arnold, R. Gaete-Holmes, A. W. Johnson, A. R. P. Smith and G. A. Williams, Wittig condensation products from nickel meso-formyl-octaethyl-porphyrin and -aetioporphyrin I and some cyclisation reactions, J. Chem. Soc., Perkin Trans. 1, 1978, 1660–1670

    Article  Google Scholar 

  111. M. O. Senge, M. D. G. H. Vicente, S. R. Parkin, H. Hope and K. M. Smith, Structural investigations on mono- and di-acrolein substituted Ni(II) porphyrins and a Ni(II) benzochlorin. model compounds for photosensitizers in photodynamic therapy, Z. Naturforsch., B: Chem. Sci., 1992, 47, 1189–1202

    Article  CAS  Google Scholar 

  112. G. Li, R. Mehta, T. Srikrishnan, D. J. Nurco, W. A. Tabaczynski, J. L. Alderfer, K. M. Smith, T. J. Dougherty and R. K. Pandey, A novel synthetic route to fused propeno-chlorin and benzochlorin photodynamic therapy probes, Chem. Commun., 2002, 1172–1173

    Google Scholar 

  113. A. Pelter, J. A. Ballantine, P. Murray-Rust, V. Ferrito and A. F. Psaila, The structures of anhydrobonellin and bonellin, the physiologically active pigment from the marine echiuroid Bonellia viridis, Tetrahedron Lett., 1978, 19, 1881–1884

    Article  Google Scholar 

  114. M. Ptaszek, D. Lahaye, M. Krayer, C. Muthiah and J. S. Lindsey, De novo synthesis of long-wavelength absorbing chlorin-13,15-dicarboximides, J. Org. Chem., 2010, 75, 1659–1673

    Article  CAS  PubMed  Google Scholar 

  115. I. Meunier, R. K. Pandey, M. O. Senge, T. J. Dougherty and K. M. Smith, Benzoporphyrin derivatives: synthesis, structure, and preliminary biological activity, J. Chem. Soc., Perkin Trans. 1, 1994, 961–969.

    Article  Google Scholar 

  116. A. F. Uchoa, K. T. de Oliveira, M. S. Baptista, A. J. Bortoluzzi, Y. Iamamoto and O. A. Serra, Chlorin photosensitizer sterically designed to prevent self-aggregation, J. Org. Chem., 2011, 76, 8824–8832

    Article  CAS  PubMed  Google Scholar 

  117. J. Akhigbe, M. Luciano, M. Zeller and C. Brückner, Mono- and bisqui-noline-annulated porphyrins from porphyrin ß,ß'-dione oximes, J. Org. Chem., 2015, 80, 499–511

    Article  CAS  PubMed  Google Scholar 

  118. A. S. Phadke, B. C. Robinson, K. M. Barkigia and J. Fajer, Synthesis of benzochlorins and rhodinobenzochlorins, Tetrahedron, 2000, 56, 7661–7666

    Article  CAS  Google Scholar 

  119. N. Hewage, M. Zeller and C. Brückner, Oxidations of chromene-annulated chlorins, Org. Biomol. Chem., 2017, 15, 396–407.

    Article  CAS  PubMed  Google Scholar 

  120. F.-P. Montforts, B. Gerlach and F. Hoper, Discovery and synthesis of less common natural hydroporphyrins, Chem. Rev., 1994, 94, 327–347.

    Article  CAS  Google Scholar 

  121. C.-Y. Chen, E. Sun, D. Fan, M. Taniguchi, B. E. McDowell, E. Yang, J. R. Diers, D. F. Bocian, D. Holten and J. S. Lindsey, Synthesis and physicochemical properties of metallobacteriochlorins, Inorg. Chem., 2012, 51, 9443–9464

    Article  CAS  PubMed  Google Scholar 

  122. Y. Liu and J. S. Lindsey, Northern-southern route to synthetic bacteriochlorins, J. Org. Chem., 2016, 81, 11882–11897

    Article  CAS  PubMed  Google Scholar 

  123. K. M. Barkigia, J. Fajer, C. K. Chang and R. Young, Models of photosynthetic chromophores. Molecular Structure and aggregation of a bacteriochlorin, J. Am. Chem. Soc., 1984, 106, 6457–6459

    Article  CAS  Google Scholar 

  124. R. K. Pandey, M. Isaac, I. MacDonald, C. J. Medforth, M. O. Senge, T. J. Dougherty and K. M. Smith, Pinacol-pinacolone rearrangements in vic-dihydroxychlorins and bacteriochlorins: Effect of substituents at the peripheral positions, J. Org. Chem., 1997, 62, 1463–1472

    Article  CAS  Google Scholar 

  125. Z. Yu and M. Ptaszek, Near-IR emissive chlorin-bacteriochlorin energy-transfer dyads with a common donor and acceptors with tunable emission wavelength, J. Org. Chem., 2013, 78, 10678–10691

    Article  CAS  PubMed  Google Scholar 

  126. N. Zhang, K. R. Reddy, J. Jiang, M. Taniguchi, R. D. Sommer and J. S. Lindsey, Elaboration of an unexplored substitution site in synthetic bacteriochlorins, J. Porphyrins Phthalocyanines, 2015, 19, 887–902

    Article  CAS  Google Scholar 

  127. J. Almeida, A. Aguiar, A. Leite, A. M. N. Silva, L. Cunha-Silva, B. de Castro, M. Rangel, G. Barone, A. C. Tome and A. M. G. Silva, 1,3-Dipolar cycloadditions with meso-tetra-arylchlorins - site selectivity and mixed bisadducts, Org. Chem. Front., 2017, 4, 534–544.

    Article  CAS  Google Scholar 

  128. R. Waditschatka, C. Kratky, B. Jaun, J. Heinzer and A. Eschenmoser, Chemistry of pyrrocorphins: structure of nickel(II)ccccc-octaethyl-pyrrocorphinate in the solid state and in solution. Observation of the inversion barrier between enantiomorphically ruffled conformers, J. Chem. Soc., Chem. Commun., 1985, 1604–1607.

    Google Scholar 

  129. K. M. Barkigia, C. K. Chang, J. Fajer and M. W. Renner, Models of heme d1. Molecular structure and NMR characterization of an iron(III) dioxoisobacteriochlorin (porphyr-indione), J. Am. Chem. Soc., 1992, 114, 1701–1707

    Article  CAS  Google Scholar 

  130. W. B. T. Cruse, P. J. Harrison and O. Kennard, Crystal and molecular structure of 2,2,8,8,12,13,17,18-octamethyl-isobacteriochlorin, J. Am. Chem. Soc., 1982, 104, 2376–2380

    Article  CAS  Google Scholar 

  131. K. M. Barkigia, J. Fajer, C. K. Chang and G. J. B. Williams, Crystal and molecular structure of the isobacteriochlorin 3,7-dimethyl-3',7'-dihydro-2,2',8,8',12,13,17,18-octaethylporphyrin. A model for sirohydrochlorin and siroheme, J. Am. Chem. Soc., 1982, 104, 315–317

    Article  CAS  Google Scholar 

  132. F.-P. Montforts, G. Mai, F. Romanowski and J. W. Bats, A convenient synthesis of the nitrite reducing cofactor heme d1 from hematoporphyrin, Tetrahedron Lett., 1993, 33, 765–768

    Article  Google Scholar 

  133. C. L. Gibson, M. J. Doyle, P. R. Raithby and A. R. Battersby, Synthesis and X-ray structure analysis of 13,17-bis(2-methoxycarbonylethyl)-12,18-bis(methoxycarbonylmethyl)-2,2,8,8,20-pentamethyl-isobacteriochlorin, J. Chem. Soc., Perkin Trans. 1, 1994, 1893–1895.

    Article  Google Scholar 

  134. C. K. Chang, K. M. Barkigia, L. K. Hanson and J. Fajer, Models of heme d1. Structure and redox chemistry of dioxoisobacteriochlorins, J. Am. Chem. Soc., 1986, 108, 1352–1354

    Article  CAS  Google Scholar 

  135. F.-P. Montforts, F. Romanowski and J. W. Bats, A simple synthesis of dioxoisobacteriochlorins from hematoporphyrin, Angew. Chem., Int. Ed. Engl., 1989, 28, 480–483

    Article  Google Scholar 

  136. H. Vu, E. Lork and F.-P. Montforts, A concise synthesis of Ni-didecarboxysirohydrochlorin hexamethylester—a model compound for key intermediates in heme d1 and heme biosynthesis, Tetrahedron Lett., 2014, 55, 6911–6914

    Article  CAS  Google Scholar 

  137. M. W. Renner, L. R. Furenlid, K. M. Barkigia, A. Forman, H.-K. Shim, D. J. Simpson, K. M. Smith and J. Fajer, Models of factor 430. Structural and spectroscopic studies of nickel(II) and nickel(I) hydroporphyrins, J. Am. Chem. Soc., 1991, 113, 6891–6898.

    Article  CAS  Google Scholar 

  138. M. Kunieda, Y. Mikata and H. Tamiaki, Regioselective transformation of octaethylporphyrin into a phytoporphyrin analogue, J. Org. Chem., 2007, 72, 7398–7401

    Article  CAS  PubMed  Google Scholar 

  139. A. Pajunen, M. E. Stapelbroek-Möllmann and P. H. Hynninen, 31,32-Didehydrorhodochlorin-15-acetic acid trimethyl ester, Acta Crystallogr., Sect. C: Cryst. Struct. Commun., 1996, 52, 743–746

    Article  Google Scholar 

  140. M. O. Senge, K. Ruhlandt-Senge and K. M. Smith, Structure and conformation of photosynthetic pigments and related compounds. 4. Two crystal forms of a chlorin - rhodochlorin XV dimethyl ester, Acta Crystallogr., Sect. C: Cryst. Struct. Commun., 1992, 48, 1810–1815.

    Article  Google Scholar 

  141. H. Scheer, in Chlorophylls and Bacteriochlorophylls, ed. B. Grimm, R.J. Porra, W. Rüdiger and H. Scheer, Springer, Dordrecht, 2006.

  142. T. Schulte, R. G. Hiller and E. Hofmann, X-ray structures of the peridinin-chlorophyll-protein reconstituted with different chlorophylls, FEBSLett., 2010, 584, 973–978.

    Article  CAS  Google Scholar 

  143. S. Mackowski, S. Wörmke, T. H. P. Brotosudarmo, C. Jung, R. G. Hiller, H. Scheer and C. Bräuchle, Energy transfer in reconstituted peridinin-chlorophyll-protein complexes: ensemble and single-molecule spectroscopy studies, Biophys. J., 2007, 93, 3249–3259

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  144. T. H. P. Brotosudarmo, S. Mackowski, E. Hofmann, R. G. Hiller, C. Bräuchle and H. Scheer, Relative binding affinities of chlorophylls in peridinin-chlorophyll-protein reconstituted with heterochlorophyllous mixtures, Photosynth. Res., 2008, 95, 247–252.

    Article  CAS  PubMed  Google Scholar 

  145. L. Mao, Y. Wang and X. Hu, n-n Stacking interactions in the peridinin-chlorophyll-protein of Amphidinium carterae, J. Phys. Chem. B, 2003, 107, 3963–3971.

    Article  CAS  Google Scholar 

  146. G. Zucchelli, D. Brogioli, A. P. Casazza, F. M. Garlaschi and R. C. Jennings, Chlorophyll ring deformation modulates Qy electronic energy in chlorophyll-protein complexes and generates spectral forms, Biophys. J., 2007, 93, 2240–2254.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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This work was supported by a grant from Science Foundation Ireland (SFI IvP 13/IA/1894).

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Gibbons, D., Flanagan, K.J., Pounot, L. et al. Structure and conformation of photosynthetic pigments and related compounds. 15. Conformational analysis of chlorophyll derivatives - implications for hydroporphyrins in vivo. Photochem Photobiol Sci 18, 1479–1494 (2019). https://doi.org/10.1039/c8pp00500a

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