Journal articles: 'Total Internal Reflection Raman Spectroscopy'

1

Woods, David A., and Colin D. Bain. "Total internal reflection Raman spectroscopy." Analyst 137, no. 1 (2012): 35–48. http://dx.doi.org/10.1039/c1an15722a.

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Talaga, David, Andrew Bremner, Thierry Buffeteau, Renaud A. L. Vallée, Sophie Lecomte, and Sébastien Bonhommeau. "Total Internal Reflection Tip-Enhanced Raman Spectroscopy of Cytochrome c." Journal of Physical Chemistry Letters 11, no. 10 (April 24, 2020): 3835–40. http://dx.doi.org/10.1021/acs.jpclett.0c00579.

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Michaels, Chris A. "Surface-sensitive Raman microscopy with total internal reflection illumination." Journal of Raman Spectroscopy 41, no. 12 (January 27, 2010): 1670–77. http://dx.doi.org/10.1002/jrs.2610.

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4

Nickolov, Z. S., J. C. Earnshaw, and J. J. McGarvey. "Water structure at interfaces studied by total internal reflection Raman spectroscopy." Colloids and Surfaces A: Physicochemical and Engineering Aspects 76 (September 1993): 41–49. http://dx.doi.org/10.1016/0927-7757(93)80059-n.

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Kivioja, Antti O., Anna-Stiina Jääskeläinen, Ville Ahtee, and Tapani Vuorinen. "Thickness measurement of thin polymer films by total internal reflection Raman and attenuated total reflection infrared spectroscopy." Vibrational Spectroscopy 61 (July 2012): 1–9. http://dx.doi.org/10.1016/j.vibspec.2012.02.014.

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Praveena, Manimunda, Kaustav Guha, Abhilash Ravishankar, Sanjay K. Biswas, Colin D. Bain, and Vikram Jayaram. "Total internal reflection Raman spectroscopy of poly(alpha-olefin) oils in a lubricated contact." RSC Adv. 4, no. 42 (2014): 22205–13. http://dx.doi.org/10.1039/c4ra02261k.

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Greene, Phillip R., and Colin D. Bain. "Total internal reflection Raman spectroscopy of barley leaf epicuticular waxes in vivo." Colloids and Surfaces B: Biointerfaces 45, no. 3-4 (November 2005): 174–80. http://dx.doi.org/10.1016/j.colsurfb.2005.08.010.

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McKee, Kristopher J., Matthew W. Meyer, and Emily A. Smith. "Near IR Scanning Angle Total Internal Reflection Raman Spectroscopy at Smooth Gold Films." Analytical Chemistry 84, no. 10 (May 3, 2012): 4300–4306. http://dx.doi.org/10.1021/ac203355a.

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Woods, David A., Jordan Petkov, and Colin D. Bain. "Surfactant adsorption by total internal reflection Raman spectroscopy. Part III: Adsorption onto cellulose." Colloids and Surfaces A: Physicochemical and Engineering Aspects 391, no. 1-3 (November 2011): 10–18. http://dx.doi.org/10.1016/j.colsurfa.2011.07.027.

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Ly, Thong Q., Fangyuan Yang, and Steven Baldelli. "In situ quantitative study of the phase transition in surfactant adsorption layers at the silica–water interface using total internal reflection Raman spectroscopy." Physical Chemistry Chemical Physics 23, no. 38 (2021): 21701–13. http://dx.doi.org/10.1039/d1cp02645c.

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Dimethyldodecylamine N-oxide (DDAO) shows high surface activity with two distinct energy states at the hydrophilic silica/aqueous solution interface studied by total internal reflection (TIR) Raman spectroscopy combined with ratiometric and kinetic analysis.

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Woods, David A., Jordan Petkov, and Colin D. Bain. "Surfactant Adsorption Kinetics by Total Internal Reflection Raman Spectroscopy. 1. Pure Surfactants on Silica." Journal of Physical Chemistry B 115, no. 22 (June 9, 2011): 7341–52. http://dx.doi.org/10.1021/jp201338s.

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12

Beattie, D. A., M. Lidström Larsson, and Allan R. Holmgren. "In situ total internal reflection Raman spectroscopy of surfactant adsorption at a mineral surface." Vibrational Spectroscopy 41, no. 2 (August 2006): 198–204. http://dx.doi.org/10.1016/j.vibspec.2006.02.003.

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13

Sommer, Andre’ J., and Mark Hardgrove. "Attenuated Total Internal Reflection Infrared Microspectroscopy For The Study Of Trace Contaminants In Aqueous Solutions." Microscopy and Microanalysis 5, S2 (August 1999): 66–67. http://dx.doi.org/10.1017/s1431927600013659.

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Over the past several years many developments have taken place in the field of molecular spectroscopy. For Raman spectroscopy many of the improvements have arisen from technological innovations that include diode-based lasers, holographic notch filters and charged coupled detectors. In contrast, a majority of the developments in infrared spectroscopy have been in the area of new sampling accessories. A major emphasis has been placed on attenuated total internal reflection (ATR) accessories. The devices are allowing infrared spectroscopy to be employed in process control environments and quality control laboratories where the method is not only robust but has the advantages of limited sample preparation and/or in situ analysis.In the realm of microspectroscopy, ATR accessories have the added advantages of providing better spatial resolution, equal to or higher S/N for equivalent sample size compared to transmission measurements and most importantly the ability to collect spectra of small samples without the adverse effect of diffraction. One accessory which was developed several years ago is known as the Split-Pea.

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Nickolov, Z. S., J. C. Earnshaw, and J. J. McGarvey. "Total internal reflection Raman spectroscopy as a method to study water structure near Langmuir-Blodgett films." Journal of Raman Spectroscopy 24, no. 7 (July 1993): 411–16. http://dx.doi.org/10.1002/jrs.1250240705.

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Jubb, Aaron M., Dominique Verreault, Ralf Posner, Louise J. Criscenti, Lynn E. Katz, and Heather C. Allen. "Sulfate adsorption at the buried hematite/solution interface investigated using total internal reflection (TIR)-Raman spectroscopy." Journal of Colloid and Interface Science 400 (June 2013): 140–46. http://dx.doi.org/10.1016/j.jcis.2013.02.031.

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16

Nyamekye, Charles K. A., Jonathan M. Bobbitt, Qiaochu Zhu, and Emily A. Smith. "The evolution of total internal reflection Raman spectroscopy for the chemical characterization of thin films and interfaces." Analytical and Bioanalytical Chemistry 412, no. 24 (March 16, 2020): 6009–22. http://dx.doi.org/10.1007/s00216-020-02510-1.

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17

Woods, David A., Jordan Petkov, and Colin D. Bain. "Surfactant Adsorption Kinetics by Total Internal Reflection Raman Spectroscopy. 2. CTAB and Triton X-100 Mixtures on Silica." Journal of Physical Chemistry B 115, no. 22 (June 9, 2011): 7353–63. http://dx.doi.org/10.1021/jp201340j.

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18

Kivioja, Antti, Timo Hartus, Tapani Vuorinen, Patrick Gane, and Anna-Stiina Jääskeläinen. "Use of Total Internal Reflection Raman (TIR) and Attenuated Total Reflection Infrared (ATR-IR) Spectroscopy to Analyze Component Separation in Thin Offset Ink Films after Setting on Coated Paper Surfaces." Applied Spectroscopy 67, no. 6 (June 2013): 661–71. http://dx.doi.org/10.1366/12-06961.

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19

Luo, Rui-qiong, Fang Wei, Shu-shi Huang, Yue-ming Jiang, Shan-lei Zhang, Wen-qing Mo, Hong Liu, and Xi Rong. "Real-Time, Label-Free Detection of Local Exocytosis Outside Pancreatic β Cells Using Laser Tweezers Raman Spectroscopy." Applied Spectroscopy 71, no. 3 (December 9, 2016): 422–31. http://dx.doi.org/10.1177/0003702816670911.

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The examination of insulin (Ins) exocytosis at the single-cell level by conventional methods, such as electrophysiological approaches, total internal reflection imaging, and two-photon imaging technology, often requires an invasive microelectrode puncture or label. In this study, high concentrations of glucose and potassium chloride were used to stimulate β cell Ins exocytosis, while low concentrations of glucose and calcium channel blockers served as the blank and negative control, respectively. Laser tweezers Raman spectroscopy (LTRS) was used to capture the possible Raman scattering signal from a local zone outside of the cell edge. The results show that the frequencies of the strong signals from the local zones outside the cellular edge in the stimulated groups are greater than those of the control. The Raman spectra from the cellular edge, Ins and cell membrane were compared. Thus, local Ins exocytosis activity outside pancreatic β cells might be observed indirectly using LTRS, a non-invasive optical method.

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Adachi, Kenta, Tomohiro Mita, Shohei Tanaka, Kensuke Honda, Suzuko Yamazaki, Masaharu Nakayama, Takeyoshi Goto, and Hitoshi Watarai. "Kinetic characteristics of enhanced photochromism in tungsten oxide nanocolloid adsorbed on cellulose substrates, studied by total internal reflection Raman spectroscopy." RSC Advances 2, no. 5 (2012): 2128. http://dx.doi.org/10.1039/c2ra00217e.

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21

Delbeck, Sven, and H. Michael Heise. "Evaluation of Opportunities and Limitations of Mid-Infrared Skin Spectroscopy for Noninvasive Blood Glucose Monitoring." Journal of Diabetes Science and Technology 15, no. 1 (June 26, 2020): 19–27. http://dx.doi.org/10.1177/1932296820936224.

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Background: A wide range of optical techniques has recently been presented for the development of noninvasive methods for blood glucose sensing based on multivariate skin spectrum analysis, and most recent studies are reviewed in short by us. The vibrational spectral fingerprints of glucose, as especially found in the mid-infrared or Raman spectrum, have been suggested for achieving largest selectivity for the development of noninvasive blood glucose methods. Methods: Here, the different aspects on integral skin measurements are presented, which are much dependent on the absorption characteristics of water as the main skin constituent. In particular, different mid-infrared measurement techniques as realized recently are discussed. The limitations of the use of the attenuated total reflection technique in particular are elaborated, and confounding skin or saliva spectral features are illustrated and discussed in the light of recently published works, claiming that the attenuated total reflection technique can be utilized for noninvasive measurements. Results: It will be shown that the penetration depth of the infrared radiation with wavelengths around 10 µm is the essential parameter, which can be modulated by different measurement techniques as with photothermal or diffuse reflection. However, the law of physics is limiting the option of using the attenuated total reflection technique with waveguides from diamond or similar optical materials. Conclusions: There are confounding features from mucosa, stratum corneum, or saliva, which have been misinterpreted for glucose measurements. Results of an earlier study with multivariate evaluation based on glucose fingerprint features are again referred to as a negative experimental proof.

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22

Plissonneau, Marie, Alexandra Madeira, David Talaga, Sébastien Bonhommeau, Laurent Servant, Renaud A. L. Vallée, Christine Labrugère, et al. "Efficient Passivation of Ag Nanowires with 11‐Mercaptoundecanoic Acid Probed Using In Situ Total‐Internal‐Reflection Surface‐Enhanced Raman Scattering Spectroscopy." ChemNanoMat 5, no. 8 (February 20, 2019): 1044–49. http://dx.doi.org/10.1002/cnma.201900068.

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23

Walch, Nik J., Alexei Nabok, Frank Davis, and Séamus P. J. Higson. "Characterisation of thin films of graphene–surfactant composites produced through a novel semi-automated method." Beilstein Journal of Nanotechnology 7 (February 8, 2016): 209–19. http://dx.doi.org/10.3762/bjnano.7.19.

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In this paper we detail a novel semi-automated method for the production of graphene by sonochemical exfoliation of graphite in the presence of ionic surfactants, e.g., sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB). The formation of individual graphene flakes was confirmed by Raman spectroscopy, while the interaction of graphene with surfactants was proven by NMR spectroscopy. The resulting graphene–surfactant composite material formed a stable suspension in water and some organic solvents, such as chloroform. Graphene thin films were then produced using Langmuir–Blodgett (LB) or electrostatic layer-by-layer (LbL) deposition techniques. The composition and morphology of the films produced was studied with SEM/EDX and AFM. The best results in terms of adhesion and surface coverage were achieved using LbL deposition of graphene(−)SDS alternated with polyethyleneimine (PEI). The optical study of graphene thin films deposited on different substrates was carried out using UV–vis absorption spectroscopy and spectroscopic ellipsometry. A particular focus was on studying graphene layers deposited on gold-coated glass using a method of total internal reflection ellipsometry (TIRE) which revealed the enhancement of the surface plasmon resonance in thin gold films by depositing graphene layers.

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Blanco-Formoso, Maria, and Ramon A. Alvarez-Puebla. "Cancer Diagnosis through SERS and Other Related Techniques." International Journal of Molecular Sciences 21, no. 6 (March 24, 2020): 2253. http://dx.doi.org/10.3390/ijms21062253.

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Cancer heterogeneity increasingly requires ultrasensitive techniques that allow early diagnosis for personalized treatment. In addition, they should preferably be non-invasive tools that do not damage surrounding tissues or contribute to body toxicity. In this context, liquid biopsy of biological samples such as urine, blood, or saliva represents an ideal approximation of what is happening in real time in the affected tissues. Plasmonic nanoparticles are emerging as an alternative or complement to current diagnostic techniques, being able to detect and quantify novel biomarkers such as specific peptides and proteins, microRNA, circulating tumor DNA and cells, and exosomes. Here, we review the latest ideas focusing on the use of plasmonic nanoparticles in coded and label-free surface-enhanced Raman scattering (SERS) spectroscopy. Moreover, surface plasmon resonance (SPR) spectroscopy, colorimetric assays, dynamic light scattering (DLS) spectroscopy, mass spectrometry or total internal reflection fluorescence (TIRF) microscopy among others are briefly examined in order to highlight the potential and versatility of plasmonics.

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Mayerhöfer, Thomas G., Susanne Pahlow, and Jürgen Popp. "Structures for surface-enhanced nonplasmonic or hybrid spectroscopy." Nanophotonics 9, no. 4 (March 18, 2020): 741–60. http://dx.doi.org/10.1515/nanoph-2020-0037.

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AbstractAbsorption, scattering, and fluorescence are processes that increase with electric field intensity. The most prominent way to enhance electric field intensity is to use localized or propagating surface plasmon polaritons (SPPs) based on metallic particles and nanostructures. In addition, several other, much less well-known, photonic structures that increase electric field intensity exist. Interference enhancement provided by thin dielectric coatings on reflective substrates is able to provide electric field intensity enhancement over the whole substrate and not only at certain hotspots, thereby being in particular suitable for the spectroscopy of thin surface layers. The same coatings on high refractive index substrates may be used for interference-enhanced total internal reflection-based spectroscopy in much the same way as Kretschmann or Otto configuration for exciting propagating SPPs. The latter configurations can also be used to launch Bloch surface waves on 1D photonic crystal structures for the enhancement of electric field intensity and thereby absorption, scattering, and fluorescence-based spectroscopies. High refractive index substrates alone can also, when nanostructured, enhance infrared absorption or Raman scattering via Mie-type resonances. As a further method, this review will cover recent developments to employ phonon polaritons in the reststrahlen region.

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26

Yui, Hiroharu, Hideyuki Fujiwara, and Tsuguo Sawada. "Spectroscopic analysis of total-internal-reflection stimulated Raman scattering from the air/water interface under the strong focusing condition." Chemical Physics Letters 360, no. 1-2 (July 2002): 53–58. http://dx.doi.org/10.1016/s0009-2614(02)00803-5.

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27

Ngo, Dien, and Steven Baldelli. "Adsorption of Dimethyldodecylamine Oxide and Its Mixtures with Triton X-100 at the Hydrophilic Silica/Water Interface Studied Using Total Internal Reflection Raman Spectroscopy." Journal of Physical Chemistry B 120, no. 48 (November 23, 2016): 12346–57. http://dx.doi.org/10.1021/acs.jpcb.6b08853.

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Grenoble, Zlata, and Steven Baldelli. "Adsorption of Benzyldimethylhexadecylammonium Chloride at the Hydrophobic Silica–Water Interface Studied by Total Internal Reflection Raman Spectroscopy: Effects of Silica Surface Properties and Metal Salt Addition." Journal of Physical Chemistry B 117, no. 34 (August 16, 2013): 9882–94. http://dx.doi.org/10.1021/jp4015096.

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29

Autefage, Hélène, Eileen Gentleman, Elena Littmann, Martin A. B. Hedegaard, Thomas Von Erlach, Matthew O’Donnell, Frank R. Burden, David A. Winkler, and Molly M. Stevens. "Sparse feature selection methods identify unexpected global cellular response to strontium-containing materials." Proceedings of the National Academy of Sciences 112, no. 14 (March 23, 2015): 4280–85. http://dx.doi.org/10.1073/pnas.1419799112.

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Despite the increasing sophistication of biomaterials design and functional characterization studies, little is known regarding cells’ global response to biomaterials. Here, we combined nontargeted holistic biological and physical science techniques to evaluate how simple strontium ion incorporation within the well-described biomaterial 45S5 bioactive glass (BG) influences the global response of human mesenchymal stem cells. Our objective analyses of whole gene-expression profiles, confirmed by standard molecular biology techniques, revealed that strontium-substituted BG up-regulated the isoprenoid pathway, suggesting an influence on both sterol metabolite synthesis and protein prenylation processes. This up-regulation was accompanied by increases in cellular and membrane cholesterol and lipid raft contents as determined by Raman spectroscopy mapping and total internal reflection fluorescence microscopy analyses and by an increase in cellular content of phosphorylated myosin II light chain. Our unexpected findings of this strong metabolic pathway regulation as a response to biomaterial composition highlight the benefits of discovery-driven nonreductionist approaches to gain a deeper understanding of global cell–material interactions and suggest alternative research routes for evaluating biomaterials to improve their design.

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Ly, Thong, and Steven Baldelli. "Cooperative Adsorption of Nonionic Triton X-100 and Dodecyldimethylamine Oxide Surfactant Mixtures at the Hydrophilic Silica–Water Interface Studied by Total Internal Reflection Raman Spectroscopy and Multivariate Curve Resolution." Journal of Physical Chemistry B 125, no. 51 (December 16, 2021): 13928–36. http://dx.doi.org/10.1021/acs.jpcb.1c08148.

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31

OSAWA, Masatoshi. "Total reflection Raman spectroscopy." Journal of the Spectroscopical Society of Japan 37, no. 3 (1988): 207–8. http://dx.doi.org/10.5111/bunkou.37.207.

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32

Tolstykh, Nadhezda D., Marek Tuhý, Anna Vymazalová, Jakub Plášil, František Laufek, Anatoly V. Kasatkin, Fabrizio Nestola, and Olga V. Bobrova. "Maletoyvayamite, Au3Se4Te6, a new mineral from Maletoyvayam deposit, Kamchatka peninsula, Russia." Mineralogical Magazine 84, no. 1 (January 21, 2020): 117–23. http://dx.doi.org/10.1180/mgm.2019.81.

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AbstractMaletoyvayamite, Au3Se4Te6, is a new mineral discovered in a heavy-mineral concentrate from the Gaching occurrence of the Maletoyvayam deposit, Kamchatka, Russia (60°19′51.87″N, 164°46′25.65″E). It forms anhedral grains (10 to 50 μm in size) and is found in intergrowths with native gold (Au–Ag), Au tellurides (calaverite), unnamed phases (AuSe, Au2TeSe and Au oxide), native tellurium, sulfosalts (tennantite, tetrahedrite, goldfieldite and watanabeite) and supergene tripuhyite. Maletoyvayamite has a good cleavage on {010} and {001}. In plane-polarised light, maletoyvayamite is grey, has strong bireflectance (grey to bluish grey), and strong anisotropy; it exhibits no internal reflections. Reflectance values for maletoyvayamite in air (Rmin,Rmax in %) are: 38.9, 39.1 at 470 nm; 39.3, 39.5 at 546 nm; 39.3, 39.6 at 589 nm; and 39.4, 39.7 at 650 nm. Sixteen electron-microprobe analyses of maletoyvayamite gave an average composition: Au 34.46, Se 16.76, Te 47.23 and S 0.84, total 99.29 wt.%, corresponding to the formula Au2.90(Se3.52S0.44)Σ3.96Te6.14 based on 13 atoms; the average of eleven analyses on synthetic analogue is: Au 34.20, Se 19.68 and Te 45.42, total 99.30 wt.%, corresponding to Au2.90Se4.16Te5.94. The calculated density is 7.98 g/cm3. The mineral is triclinic, space group P1, with a = 8.901(2), b = 9.0451(14), c = 9.265(4) Å, α = 97.66(3), β = 106.70(2), γ = 101.399(14)°, V = 685.9(4) Å3 and Z = 2. The crystal structure of maletoyvayamite represents a unique structure type resembling a molecular structure. There are cube-like [Au6Se8Te12] clusters linked via van der Waals interactions. The structural identity of maletoyvayamite with the synthetic Au3Se4Te6 was confirmed by powder X-ray diffraction and Raman spectroscopy.

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33

Tisinger, L. G., and A. J. Sommer. "Attenuated Total Internal Reflection (ATR) Raman Microspectroscopy." Microscopy and Microanalysis 10, S02 (August 2004): 1318–19. http://dx.doi.org/10.1017/s1431927604884794.

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34

Futamata, Masayuki, and Andreas Bruckbauer. "Attenuated Total Reflection-Scanning Near-Field Raman Spectroscopy." Japanese Journal of Applied Physics 40, Part 1, No. 6B (June 30, 2001): 4423–29. http://dx.doi.org/10.1143/jjap.40.4423.

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35

Thompson, N. "Total Internal Reflection with Fluorescence Correlation Spectroscopy." Microscopy and Microanalysis 17, S2 (July 2011): 38–39. http://dx.doi.org/10.1017/s1431927611001061.

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36

Thompson, Nancy. "Total Internal Reflection with Fluorescence Correlation Spectroscopy." Biophysical Journal 102, no. 3 (January 2012): 20a. http://dx.doi.org/10.1016/j.bpj.2011.11.131.

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37

Thompson, Nancy L., and Bridgett L. Steele. "Total internal reflection with fluorescence correlation spectroscopy." Nature Protocols 2, no. 4 (April 2007): 878–90. http://dx.doi.org/10.1038/nprot.2007.110.

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Akai, Keitaro, Chiaki Iida, and Masayuki Futamata. "Gap mode Raman spectroscopy under attenuated total reflection geometry." Journal of Optics 17, no. 11 (October 23, 2015): 114008. http://dx.doi.org/10.1088/2040-8978/17/11/114008.

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39

Toriumi, Minoru, Masatoshi Yanagimachi, and Hiroshi Masuhara. "Absorption effects on total-internal-reflection fluorescence spectroscopy." Applied Optics 31, no. 30 (October 20, 1992): 6376. http://dx.doi.org/10.1364/ao.31.006376.

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40

Woods, David A., and Colin D. Bain. "Total internal reflection spectroscopy for studying soft matter." Soft Matter 10, no. 8 (2014): 1071. http://dx.doi.org/10.1039/c3sm52817k.

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41

Antipenko, A. G., V. P. Novikov, and M. A. Novikov. "Optoacoustic methods using total internal reflection." Journal of Applied Spectroscopy 43, no. 4 (October 1985): 1159–62. http://dx.doi.org/10.1007/bf00662336.

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42

McKee, Kristopher J., and Emily A. Smith. "Development of a scanning angle total internal reflection Raman spectrometer." Review of Scientific Instruments 81, no. 4 (April 2010): 043106. http://dx.doi.org/10.1063/1.3378682.

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43

Lieto, Alena M., and Nancy L. Thompson. "Total Internal Reflection with Fluorescence Correlation Spectroscopy: Nonfluorescent Competitors." Biophysical Journal 87, no. 2 (August 2004): 1268–78. http://dx.doi.org/10.1529/biophysj.103.035030.

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44

Leutenegger, Marcel, Hans Blom, Jerker Widengren, Christian Eggeling, Michael Gösch, Rainer A. Leitgeb, and Theo Lasser. "Dual-color total internal reflection fluorescence cross-correlation spectroscopy." Journal of Biomedical Optics 11, no. 4 (2006): 040502. http://dx.doi.org/10.1117/1.2221714.

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45

Sanchez, Esaul, Ping Shaw, James A. O’Neill, and Richard M. Osgood. "Infrared total internal reflection spectroscopy of dimethylcadmium on silicon." Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films 6, no. 3 (May 1988): 765–67. http://dx.doi.org/10.1116/1.575104.

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46

Otosu, Takuhiro, and Shoichi Yamaguchi. "Total Internal Reflection Two-Dimensional Fluorescence Lifetime Correlation Spectroscopy." Journal of Physical Chemistry B 122, no. 22 (May 25, 2018): 5758–64. http://dx.doi.org/10.1021/acs.jpcb.8b01176.

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47

Li, Meng, Tinglian Yuan, Yingyan Jiang, Linlin Sun, Wei Wei, Hong-Yuan Chen, and Wei Wang. "Total Internal Reflection-Based Extinction Spectroscopy of Single Nanoparticles." Angewandte Chemie 131, no. 2 (November 21, 2018): 582–86. http://dx.doi.org/10.1002/ange.201810324.

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48

Li, Meng, Tinglian Yuan, Yingyan Jiang, Linlin Sun, Wei Wei, Hong-Yuan Chen, and Wei Wang. "Total Internal Reflection-Based Extinction Spectroscopy of Single Nanoparticles." Angewandte Chemie International Edition 58, no. 2 (November 21, 2018): 572–76. http://dx.doi.org/10.1002/anie.201810324.

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49

Ishizaki, Fumihiko, and Munsok Kim. "Near-Infrared Attenuated Total Reflection Raman Spectroscopy for Polymer Surface Observation." Japanese Journal of Applied Physics 47, no. 3 (March 14, 2008): 1621–27. http://dx.doi.org/10.1143/jjap.47.1621.

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50

Heidari, Alireza. "Vibrational biospectroscopic study and chemical structure analysis of unsaturated polyamides nanoparticles as anti–cancer polymeric nanomedicines using synchrotron radiation." International Journal of Advanced Chemistry 6, no. 2 (August 4, 2018): 167. http://dx.doi.org/10.14419/ijac.v6i2.12528.

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Firstly, unsaturated polyamides nanoparticles were hardened by continuous synchrotron radiation and then, the induced changes in its chemical structure were studied by Attenuated Total Reflection–Fourier Transform Infrared (ATR–FTIR) spectroscopy. It was shown that applying synchrotron radiation for hardening not only leads to reduction of hardening time but also creates cross link in polymer by breaking Carbon–Carbon double bond, without any considerable change in its chemical structure. In addition, an unsaturated polyamide nanoparticle as anti–cancer polymeric nanomedicines is hardened by synchrotron radiation. Its chemical structure before and after hardening is studied using Raman and Attenuated Total Reflection–Fourier Transform Infrared (ATR–FTIR) spectroscopy. The results show that Raman spectroscopy is considerably better than Attenuated Total Reflection–Fourier Transform Infrared (ATR–FTIR) spectroscopy in detecting the changes happened in chemical structure.

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Journal articles on the topic 'Total Internal Reflection Raman Spectroscopy'

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