11 Fluorescent Chemosensors
407
Niko Y, Kawauchi S, Konishi GI (2013) Solvatochromic pyrene analogues of prodan exhibiting
extremely high fluorescence quantum yields in apolar and polar solvents. Chem A Eur J 19:9760–
9765. https://doi.org/10.1002/chem.201301020
Niko Y, Arntz Y, Mely Y, Konishi GI, Klymchenko AS (2014) Disassembly-driven fluorescence
turn-on of polymerized micelles by reductive stimuli in living cells. Chem A Eur J 20:16473–
16477. https://doi.org/10.1002/chem.201405040
Niko Y, Sasaki S, Narushima K, Sharma DK, Vacha M, Konishi GI (2015) 1-, 3-, 6-, and 8tetrasubstituted asymmetric pyrene derivatives with electron donors and acceptors: high photostability and regioisomer-specific photophysical properties. J Org Chem 80:10794–10805. https://
doi.org/10.1021/acs.joc.5b01987
Pawlicki M, Collins HA, Denning RG, Anderson HL (2009) Two-photon absorption and the
design of two-photon dyes. Angew Chemie Int Ed 48:3244–3266. https://doi.org/10.1002/anie.
200805257
Reichardt C (2005) Solvatochromic dyes as solvent polarity indicators. Chem Rev 94:2319–2358.
https://doi.org/10.1021/cr00032a005
Reisch A, Klymchenko AS (2016) Fluorescent polymer nanoparticles based on dyes: seeking
brighter tools for bioimaging. Small 12:1968–1992. https://doi.org/10.1002/smll.201503396
Rice TE, McCoy CP, Gunaratne HQN, de Silva AP, Rademacher JT, Huxley AJM, Gunnlaugsson T
(2002) Signaling recognition events with fluorescent sensors and switches. Chem Rev 97:1515–
1566. https://doi.org/10.1021/cr960386p
Sahoo H (2011) Förster resonance energy transfer—a spectroscopic nanoruler: principle and applications. J Photochem Photobiol C Photochem Rev 12:20–30. https://doi.org/10.1016/j.jphotoche
mrev.2011.05.001
Sale P, Montalti M, Farruggia G, Wolf FI, Prodi L, Zaccheroni N, Savage PB, Iotti S, Trapani V
(2006) 8-hydroxyquinoline derivatives as fluorescent sensors for magnesium in living cells. J Am
Chem Soc 128:344–350. https://doi.org/10.1021/ja056523u
Sapsford KE, Algar WR, Berti L, Gemmill KB, Casey BJ, Oh E, Stewart MH, Medintz IL (2013)
Functionalizing nanoparticles with biological molecules: developing chemistries that facilitate
nanotechnology. Chem Rev 113:1904–2074. https://doi.org/10.1021/cr300143v
Schuster R (1988) Determination of amino acids in biological, pharmaceutical, plant and food
samples by automated precolumn derivatization and high-performance liquid chromatography. J
Chromatogr B Biomed Sci Appl 431:271–284. https://doi.org/10.1016/S0378-4347(00)83096-0
Sekida S, Kameyama T, Koga T, Hadano S, Watanabe S, Niko Y (2018) Highly lipophilic and
solid emissive N-annulated perylene bisimide synthesis for facile preparation of bright and farred excimer fluorescent nano-emulsions with large Stokes shift. J Photochem Photobiol A Chem
364:16–21. https://doi.org/10.1016/j.jphotochem.2018.05.023
Shweta KA, Neeraj ASK, Prakash A, Roy JK, Tiwari I, Upadhyay KK (2016) A highly sensitive naphthaoxazole-based cell-permeable ratiometric chemodosimeter for hydrazine. RSC Adv
6:94959–94966. https://doi.org/10.1039/c6ra15081k
Smith AM, Mancini MC, Nie S (2009) Bioimaging: second window for in vivo imaging. Nat
Nanotechnol 4:710–711. https://doi.org/10.1038/nnano.2009.326
Soper SA, Nutter HL, Keller RA, Davis LM, Shera EB (1993) The photophysical constants of several
fluorescent dyes pertaining to ultrasensitive fluorescence spectroscopy. Photochem Photobiol
57:972–977. https://doi.org/10.1111/j.1751-1097.1993.tb02957.x
Sousa LR, Larson JM (1977) Crown ether model systems for the study of photoexcited state response
to geometrically oriented perturbers. The effect of alkali metal ions on emission from naphthalene
derivatives. J Am Chem Soc 99:307–310. https://doi.org/10.1021/ja00443a084
Spano FC, Introduction I (2009) The spectral signatures of frenkel polarons in. Acc Chem Res
43:429–439. https://doi.org/10.1021/ar900233v
Tsien RY (1980) new calcium indicators and buffers with high selectivity against magnesium and
protons: design, synthesis, and properties of prototype structures. Biochemistry 19:2396–2404.
https://doi.org/10.1021/bi00552a018
407
Niko Y, Kawauchi S, Konishi GI (2013) Solvatochromic pyrene analogues of prodan exhibiting
extremely high fluorescence quantum yields in apolar and polar solvents. Chem A Eur J 19:9760–
9765. https://doi.org/10.1002/chem.201301020
Niko Y, Arntz Y, Mely Y, Konishi GI, Klymchenko AS (2014) Disassembly-driven fluorescence
turn-on of polymerized micelles by reductive stimuli in living cells. Chem A Eur J 20:16473–
16477. https://doi.org/10.1002/chem.201405040
Niko Y, Sasaki S, Narushima K, Sharma DK, Vacha M, Konishi GI (2015) 1-, 3-, 6-, and 8tetrasubstituted asymmetric pyrene derivatives with electron donors and acceptors: high photostability and regioisomer-specific photophysical properties. J Org Chem 80:10794–10805. https://
doi.org/10.1021/acs.joc.5b01987
Pawlicki M, Collins HA, Denning RG, Anderson HL (2009) Two-photon absorption and the
design of two-photon dyes. Angew Chemie Int Ed 48:3244–3266. https://doi.org/10.1002/anie.
200805257
Reichardt C (2005) Solvatochromic dyes as solvent polarity indicators. Chem Rev 94:2319–2358.
https://doi.org/10.1021/cr00032a005
Reisch A, Klymchenko AS (2016) Fluorescent polymer nanoparticles based on dyes: seeking
brighter tools for bioimaging. Small 12:1968–1992. https://doi.org/10.1002/smll.201503396
Rice TE, McCoy CP, Gunaratne HQN, de Silva AP, Rademacher JT, Huxley AJM, Gunnlaugsson T
(2002) Signaling recognition events with fluorescent sensors and switches. Chem Rev 97:1515–
1566. https://doi.org/10.1021/cr960386p
Sahoo H (2011) Förster resonance energy transfer—a spectroscopic nanoruler: principle and applications. J Photochem Photobiol C Photochem Rev 12:20–30. https://doi.org/10.1016/j.jphotoche
mrev.2011.05.001
Sale P, Montalti M, Farruggia G, Wolf FI, Prodi L, Zaccheroni N, Savage PB, Iotti S, Trapani V
(2006) 8-hydroxyquinoline derivatives as fluorescent sensors for magnesium in living cells. J Am
Chem Soc 128:344–350. https://doi.org/10.1021/ja056523u
Sapsford KE, Algar WR, Berti L, Gemmill KB, Casey BJ, Oh E, Stewart MH, Medintz IL (2013)
Functionalizing nanoparticles with biological molecules: developing chemistries that facilitate
nanotechnology. Chem Rev 113:1904–2074. https://doi.org/10.1021/cr300143v
Schuster R (1988) Determination of amino acids in biological, pharmaceutical, plant and food
samples by automated precolumn derivatization and high-performance liquid chromatography. J
Chromatogr B Biomed Sci Appl 431:271–284. https://doi.org/10.1016/S0378-4347(00)83096-0
Sekida S, Kameyama T, Koga T, Hadano S, Watanabe S, Niko Y (2018) Highly lipophilic and
solid emissive N-annulated perylene bisimide synthesis for facile preparation of bright and farred excimer fluorescent nano-emulsions with large Stokes shift. J Photochem Photobiol A Chem
364:16–21. https://doi.org/10.1016/j.jphotochem.2018.05.023
Shweta KA, Neeraj ASK, Prakash A, Roy JK, Tiwari I, Upadhyay KK (2016) A highly sensitive naphthaoxazole-based cell-permeable ratiometric chemodosimeter for hydrazine. RSC Adv
6:94959–94966. https://doi.org/10.1039/c6ra15081k
Smith AM, Mancini MC, Nie S (2009) Bioimaging: second window for in vivo imaging. Nat
Nanotechnol 4:710–711. https://doi.org/10.1038/nnano.2009.326
Soper SA, Nutter HL, Keller RA, Davis LM, Shera EB (1993) The photophysical constants of several
fluorescent dyes pertaining to ultrasensitive fluorescence spectroscopy. Photochem Photobiol
57:972–977. https://doi.org/10.1111/j.1751-1097.1993.tb02957.x
Sousa LR, Larson JM (1977) Crown ether model systems for the study of photoexcited state response
to geometrically oriented perturbers. The effect of alkali metal ions on emission from naphthalene
derivatives. J Am Chem Soc 99:307–310. https://doi.org/10.1021/ja00443a084
Spano FC, Introduction I (2009) The spectral signatures of frenkel polarons in. Acc Chem Res
43:429–439. https://doi.org/10.1021/ar900233v
Tsien RY (1980) new calcium indicators and buffers with high selectivity against magnesium and
protons: design, synthesis, and properties of prototype structures. Biochemistry 19:2396–2404.
https://doi.org/10.1021/bi00552a018