Fluorescence Quantum Yields of a Series of Red and Near-Infrared Dyes Emitting at 600−1000 nm

Knut Rurack; Monika Spieles

doi:10.1021/ac101329h

journal article Jan 20, 2011

Fluorescence Quantum Yields of a Series of Red and Near-Infrared Dyes Emitting at 600−1000 nm

Knut Rurack Monika Spieles

Analytical Chemistry Vol. 83 No. 4 pp. 1232-1242 · American Chemical Society (ACS)

View at Publisher Save 10.1021/ac101329h

Topics

No keywords indexed for this article. Browse by subject →

References

76

[1]

Lakowicz J. R. (1992)

[2]

Wolfbeis O. S. (2001)

[3]

Pawley J. B. (2006) 10.1007/978-0-387-45524-2

[4]

Miller L. W. (2008) 10.1002/9783527623099

[5]

Demchenko A. (2009) 10.1007/978-1-4020-9003-5

[6]

Lakowicz J. R. (2006) 10.1007/978-0-387-46312-4

[7]

Valeur B. (2001) 10.1002/3527600248

[8]

Gonçalves M. S. T. Chem. Rev. (2009) 10.1021/cr0783840

[9]

Borisov S. M. Analyst (2008) 10.1039/b805432k

[10]

Zheng J. Annu. Rev. Phys. Chem. (2007) 10.1146/annurev.physchem.58.032806.104546

[11]

Wolff M. Comb. Chem. High Throughput Screening (2008) 10.2174/138620708785739880

[12]

Resch-Genger U. Nat. Methods (2008) 10.1038/nmeth.1248

[13]

Thomas S. W. Chem. Rev. (2007) 10.1021/cr0501339

[14]

Rurack K. Springer Ser. Fluoresc. (2008) 10.1007/4243_2008_019

[15]

Demas, J. N.InMeasurement of Photolouminescence, Optical Radiation Measurements;Mielenz, K. D., Ed.Academic:New York, 1982; Vol.3, pp195−248.

[16]

Velapoldi R. A. (1980)

[17]

Parker C. A. Analyst (1960) 10.1039/an9608500587

[18]

Braslavsky S. E. Pure Appl. Chem. (2007) 10.1351/pac200779030293

[19]

DeRose P. C. Springer Ser. Fluoresc. (2008) 10.1007/4243_2008_049

[20]

Dittrich P. S. Anal. Bioanal. Chem. (2005) 10.1007/s00216-005-3335-9

[21]

Seidel M. Anal. Bioanal. Chem. (2008) 10.1007/s00216-008-2039-3

[22]

Petty H. R. Microsc. Res. Tech. (2007) 10.1002/jemt.20455

[23]

Sako Y. Cell Struct. Funct. (2002) 10.1247/csf.27.357

[24]

Reits E. A. J. Nat. Cell Biol. (2001) 10.1038/35078615

[25]

Erickson S. J. Med. Eng. Phys. (2009) 10.1016/j.medengphy.2008.10.004

[26]

Wessels J. T. Cytometry (2007) 10.1002/cyto.a.20419

[27]

Weissleder R. Nat. Biotechnol. (2001) 10.1038/86684

[28]

Achilefu S. Technol. Cancer Res. Treat. (2004) 10.1177/153303460400300410

[29]

Kiyose K. Chem. Asian J. (2008) 10.1002/asia.200700267

[30]

Descalzo A. B. Ann. N.Y. Acad. Sci. (2008) 10.1196/annals.1430.016

[31]

Amiot C. L. Sensors (2008) 10.3390/s8053082

[32]

Miller J. N. Springer Ser. Fluoresc. (2008) 10.1007/4243_2008_057

[33]

Galanin M. D. Opt. Spectrosc. (1982)

[34]

Bindhu C. V. Anal. Sci. (2001) 10.2116/analsci.17.141

[35]

Benson R. C. J. Chem. Eng. Data (1977) 10.1021/je60075a020

[36]

Certificate of Analysis, Standard Reference Material SRM 936a, Quinine Sulfate Dihydrate. National Institute of Standards and Technology: Gaithersburg, MD, 1994.https://www-s.nist.gov/srmors/view_detail.cfm?srm=936A(accessed Dec 1, 2010) .Note that, according to NIST’s website, this SRM is currently out of stock.

[37]

Hollandt J. J. Fluoresc. (2005) 10.1007/s10895-005-2628-x

[38]

Resch-Genger U. J Fluoresc. (2005) 10.1007/s10895-005-2629-9

[39]

Pfeifer D. J. Fluoresc. (2006) 10.1007/s10895-006-0086-8

[40]

bUpdated, see: BAM-F001,F002a,F003-F005, Calibration Kit, Spectral Fluorescence Standards; BAM Federal Institute for Materials Research and Testing: Berlin, 2009.http://www.comar.bam.de/home/search_crm.php(accessed Dec 1, 2010) .

[41]

cResch-Genger, U.; Pfeifer, D.; Monte, C.; Hoffmann, A.; Nording, P.; Schönenberger, B.; Hoffmann, K.; Spieles, M.; Rurack, K.German Patent DE 10 2004 044 717, 2010; U.S. Patent US 2010/0219333, 2010.

[42]

Monte C. Metrologia (2006) 10.1088/0026-1394/43/2/s18

[43]

Descalzo A. B. Chem.—Eur. J. (2009) 10.1002/chem.200802087

[44]

Slominskii Y. L. Ukr. Khim. Zh. (1984)

[45]

Grabolle M. Anal. Chem. (2009) 10.1021/ac900308v

[46]

Demas J. N. Anal. Chem. (1973) 10.1021/ac60328a014

[47]

Landolt−Börnstein compendium.http://www.springermaterials.com/navigation/(accessed Dec 1, 2010) .

[48]

Drexhage K. H. J. Res. Natl. Bur. Stand. (1976) 10.6028/jres.080a.044

[49]

Karstens T. J. Phys. Chem. (1980) 10.1021/j100451a030

[50]

Galanin M. D. Opt. Spectrosc. (1982)

Showing 50 of 76 references

Cited By

667

Development of AS1411 aptamer-conjugated chitosan-carbon dot nanocarriers for targeted drug delivery and fluorescent imaging in breast cancer therapy

Mohammad Jafar Mantashlou, Effat Alizadeh · 2026

Journal of Biological Engineering

Optical properties of novel coumarin-fused pyrano-pyridines: synthesis and TD-DFT calculations

Faeze Roshan Shokranlu, Mohammad Izadyar · 2026

Journal of Molecular Structure

Dicyanoisophorone-based near-infrared fluorescent probe with a large Stokes shift for the detection and bioimaging of hydrazine

Hong-Cheng Xia, Yu-Hang Zhang · 2026

Journal of Hazardous Materials

Steering Energy Transfer Pathways through Mn-Doping in Perovskite Nanocrystals

Akshaya Chemmangat, Sara Murray · 2025

Journal of the American Chemical So...

Scalable fabrication and characterization of high refractive index luminescent dye-doped polymer films for planar waveguides and thermal imprint

Ł. Duda, M. Czajkowski · 2025

Dyes and Pigments

Dinuclear Heteroleptic Erbium Complexes for Improving Molecular-Based Light Upconversion in Solution?

Inès Taarit, Quentin Sommer · 2025

Inorganic Chemistry

Mixed halide perovskite-based luminescent solar concentrator with high efficiency

Ali Mehdipour-Sorayaei, Farhad Sattari · 2024

Journal of Molecular Structure

Enhanced Antibacterial Activity of Novel Fluorescent Glutathione-Capped Ag Nanoclusters

Roman Tumskiy, Boris Khlebtsov · 2023

International Journal of Molecular...

Expedient Synthesis of Oxaboracyclic Compounds Based on Naphthalene and Biphenyl Backbone and Phase‐Dependent Luminescence of their Chelate Complexes

Krzysztof Durka, Paulina H. Marek‐Urban · 2022

Chemistry – A European Journal

Shedding light on ultrafast ring-twisting pathways of halogenated GFP chromophores from the excited to ground state

Sean A. Boulanger, Cheng Chen · 2021

Physical Chemistry Chemical Physics

Illuminating Excited-State Intramolecular Proton Transfer of a Fungi-Derived Red Pigment for Sustainable Functional Materials

Taylor D. Krueger, Janak Solaris · 2021

The Journal of Physical Chemistry C

A Novel Dialkylamino GFP Chromophore as an Environment-Polarity Sensor Reveals the Role of Twisted Intramolecular Charge Transfer

Cheng Chen, Sean A. Boulanger · 2021

Chemosensors

Near-Infrared-Emitting Hemicyanines and Their Photodynamic Killing of Cancer Cells

Mithun Santra, Matthew Owens · 2021

ACS Applied Bio Materials

Effects of Viscosity and Refractive Index on the Emission and Diffusion Properties of Alexa Fluor 405 Using Fluorescence Correlation and Lifetime Spectroscopies

Camila van Zanten, Dzmitry Melnikau · 2021

Journal of Fluorescence

Discovering a rotational barrier within a charge-transfer state of a photoexcited chromophore in solution

Taylor D. Krueger, Sean A. Boulanger · 2020

Structural Dynamics

Spectral Properties of Indotricarbocyanine Dye during Self-Assembly of Its H*- and J-Aggregates

N. V. Belko, M. P. Samtsov · 2020

Optics and Spectroscopy

Predicting fluorescence quantum yields for molecules in solution: A critical assessment of the harmonic approximation and the choice of the lineshape function

Alexander Humeniuk, Margarita Bužančić · 2020

The Journal of Chemical Physics

Efficient and Selective Conversion of Phosphine-Protected (MAu8)2+ (M = Pd, Pt) Superatoms to Thiolate-Protected (MAu12)6+ or Alkynyl-Protected (MAu12)4+ Superatoms via Hydride Doping

Shinjiro Takano, Shun Ito · 2019

Journal of the American Chemical So...

Extended Triangulenium Ions: Syntheses and Characterization of Benzo-Bridged Dioxa- and Diazatriangulenium Dyes

Martin Rosenberg, Marco Santella · 2019

The Journal of Organic Chemistry

Deciphering and quantifying linear light upconversion in molecular erbium complexes

Bahman Golesorkhi, Alexandre Fürstenberg · 2019

Chemical Science

Metrics

667

Citations

76

References

Details

Published: Jan 20, 2011
Vol/Issue: 83(4)
Pages: 1232-1242

Authors

K

Knut Rurack

Division 1.5 Bioanalytics, BAM Bundesanstalt für Materialforschung und -prüfung, Richard-Willstätter-Strasse 11, D-12489 Berlin, Germany

M

Monika Spieles

Division 1.5 Bioanalytics, BAM Bundesanstalt für Materialforschung und -prüfung, Richard-Willstätter-Strasse 11, D-12489 Berlin, Germany

Cite This Article

Knut Rurack, Monika Spieles (2011). Fluorescence Quantum Yields of a Series of Red and Near-Infrared Dyes Emitting at 600−1000 nm. Analytical Chemistry, 83(4), 1232-1242. https://doi.org/10.1021/ac101329h

Fluorescence Quantum Yields of a Series of Red and Near-Infrared Dyes Emitting at 600−1000 nm

You May Also Like