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Journal articles on the topic '17-O nmr'

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Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Cerioni, Giovanni, Nicola Culeddu, and Antonio Saba. "O-17 NMR studies on ?-diazoketones." Journal of Physical Organic Chemistry 5, no. 7 (July 1992): 424–28. http://dx.doi.org/10.1002/poc.610050706.

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2

Gierczyk, Błażej, Maciej Zalas, Marcin Kaźmierczak, Jakub Grajewski, Radosław Pankiewicz, and Bożena Wyrzykiewicz. "17 O NMR studies of substituted 1,3,4-oxadiazoles." Magnetic Resonance in Chemistry 49, no. 10 (September 15, 2011): 648–54. http://dx.doi.org/10.1002/mrc.2804.

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3

ZEYER, MICHAELA, LIONEL MONTAGNE, CHRISTIAN JÄGER, and GERARD PALAVIT. "¹⁷O NMR OF CRYSTALLINE SODIUM TRIMETAPHOSPHATE." Phosphorus Research Bulletin 13 (2002): 275–78. http://dx.doi.org/10.3363/prb1992.13.0_275.

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4

Wzietek, P., D. Köngeter, P. Auban, D. Jérome, J. M. Bassat, J. P. Coutures, B. Dubois, and Ph Odier. "17 O NMR in YBa 2 Cu 3 O 7-δ Superconductors." Europhysics Letters (EPL) 8, no. 4 (February 15, 1989): 363–68. http://dx.doi.org/10.1209/0295-5075/8/4/011.

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5

Takigawa, M., P. C. Hammel, R. H. Heffner, Z. Fisk, K. C. Ott, and J. D. Thompson. "17 O NMR study of YBa 2 Cu 3 O 7−δ." Physica C: Superconductivity and its Applications 162-164 (December 1989): 853–56. http://dx.doi.org/10.1016/0921-4534(89)90492-9.

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6

Cerioni, Giovanni, Nicola Culeddu, and Antonio Plumitallo. "C-13 and O-17 NMR studies on N-sulfinylanilines." Tetrahedron 49, no. 14 (April 1993): 2957–64. http://dx.doi.org/10.1016/s0040-4020(01)80390-2.

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7

Pace, Vittorio, Wolfgang Holzer, Laura Ielo, Shicheng Shi, Guangrong Meng, Mina Hanna, Roman Szostak, and Michal Szostak. "17O NMR and15N NMR chemical shifts of sterically-hindered amides: ground-state destabilization in amide electrophilicity." Chemical Communications 55, no. 30 (2019): 4423–26. http://dx.doi.org/10.1039/c9cc01402k.

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We report¹⁷O NMR and¹⁵N NMR spectroscopic data for sterically-hindered acyclic amides. The data demonstrate that a combined use of¹⁷O NMR and¹⁵N NMR serves as a powerful tool in assessing electronic effects of the amide bond.

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8

Kitaoka, Y., Y. Berthier, P. Butaud, M. Horvatić, P. Ségransan, C. Berthier, H. Katayama-Yoshida, Y. Okabe, and T. Takahashi. "NMR study of 17 O in high T c superconducting oxides." Physica C: Superconductivity and its Applications 162-164 (December 1989): 195–96. http://dx.doi.org/10.1016/0921-4534(89)90984-2.

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9

Ogloblichev, Vasily V., Alexey G. Smolnikov, Almaz F. Sadykov, Yuri V. Piskunov, Alexander P. Gerashenko, Yuji Furukawa, Ken-ichi Kumagai, et al. "17 O NMR study of the triangular lattice antiferromagnet CuCrO 2." Journal of Magnetism and Magnetic Materials 458 (July 2018): 1–9. http://dx.doi.org/10.1016/j.jmmm.2018.02.080.

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10

Zhu, Xiao-Hong, Yi Zhang, Hannes M. Wiesner, Kamil Ugurbil, and Wei Chen. "In vivo measurement of CBF using 17 O NMR signal of metabolically produced H2 17 O as a perfusion tracer." Magnetic Resonance in Medicine 70, no. 2 (September 21, 2012): 309–14. http://dx.doi.org/10.1002/mrm.24469.

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11

Fusaro, Luca, Giulia Mameli, Francesca Mocci, Michel Luhmer, and Giovanni Cerioni. "Dynamic NMR of low-sensitivity fast-relaxing nuclei: 17 O NMR and DFT study of acetoxysilanes." Magnetic Resonance in Chemistry 50, no. 2 (February 2012): 152–58. http://dx.doi.org/10.1002/mrc.3794.

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12

CERIONI, G., N. CULEDDU, and A. PLUMITALLO. "ChemInform Abstract: C-13 and O-17 NMR Studies on N-Sulfinylanilines." ChemInform 24, no. 30 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199330035.

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13

Nummert, Vilve, Vahur Mäemets, Mare Piirsalu, and Ilmar A. Koppel. "17 O NMR studies of ortho -substituent effects in substituted phenyl tosylates." Magnetic Resonance in Chemistry 50, no. 10 (August 31, 2012): 696–704. http://dx.doi.org/10.1002/mrc.3864.

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14

Ando, Mariko, Itaru Oikawa, Yasuto Noda, Shinobu Ohki, Masataka Tansho, Tadashi Shimizu, Hajime Kiyono, and Hideki Maekawa. "High field O-17 NMR study of defects in doped zirconia and ceria." Solid State Ionics 192, no. 1 (June 2011): 576–79. http://dx.doi.org/10.1016/j.ssi.2010.04.024.

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15

Elliott, Stuart James, Christian Bengs, Karel Kouril, Benno Meier, Shamim Alom, Richard John Whitby, and Malcolm Harris Levitt. "NMR Lineshapes and Scalar Relaxation of the Water-Endofullerene H2 17 O@C60." ChemPhysChem 19, no. 3 (February 5, 2018): 251–55. http://dx.doi.org/10.1002/cphc.201701330.

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16

Chen, Chia‐Hsin, Frederic Mentink‐Vigier, Julien Trébosc, Ieva Goldberga, Philippe Gaveau, Emilie Thomassot, Dinu Iuga, et al. "Labeling and Probing the Silica Surface Using Mechanochemistry and 17 O NMR Spectroscopy**." Chemistry – A European Journal 27, no. 49 (July 22, 2021): 12574–88. http://dx.doi.org/10.1002/chem.202101421.

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17

Klein, Brittney A., Dylan G. Tkachuk, Victor V. Terskikh, and Vladimir K. Michaelis. "Expanding the NMR toolkit for biological solids: oxygen-17 enriched Fmoc-amino acids." New Journal of Chemistry 45, no. 28 (2021): 12384–98. http://dx.doi.org/10.1039/d1nj02847b.

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18

Ielo, Laura, Vittorio Pace, Wolfgang Holzer, Md Mahbubur Rahman, Guangrong Meng, Roman Szostak, and Michal Szostak. "Electrophilicity Scale of Activated Amides: 17 O NMR and 15 N NMR Chemical Shifts of Acyclic Twisted Amides in N−C(O) Cross‐Coupling." Chemistry – A European Journal 26, no. 69 (November 11, 2020): 16246–50. http://dx.doi.org/10.1002/chem.202003213.

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19

Sasaki, Yoshihiro, Noboru Yoshimura, and Yoshio Takahashi. "Effect of Far Infrared Radiation on Water Clusters Analyzed ¹⁷O-NMR." JOURNAL OF THE ILLUMINATING ENGINEERING INSTITUTE OF JAPAN 77, no. 2 (1993): 95–101. http://dx.doi.org/10.2150/jieij1980.77.2_95.

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20

Lippmaa, Endel, Enno Joon, Ivo Heinmaa, Andrus Miller, Veiko Miidel, Raivo Stern, and Sirje Vija. "NMR of 17 O and 63 Cu in uniaxially aligned superconductor YBa 2 Cu 3 O 7-δ." Physica C: Superconductivity and its Applications 162-164 (December 1989): 263–64. http://dx.doi.org/10.1016/0921-4534(89)91018-6.

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21

Ashbrook, Sharon E., Zachary H. Davis, Russell E. Morris, and Cameron M. Rice. "17O NMR spectroscopy of crystalline microporous materials." Chemical Science 12, no. 14 (2021): 5016–36. http://dx.doi.org/10.1039/d1sc00552a.

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Cost-effective and atom-efficient isotopic enrichment enables ¹⁷O NMR spectroscopy of microporous materials to be used to probe local structure and disorder and to explore chemical reactivity.

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22

Brownbill, Nick J., David Gajan, Anne Lesage, Lyndon Emsley, and Frédéric Blanc. "Oxygen-17 dynamic nuclear polarisation enhanced solid-state NMR spectroscopy at 18.8 T." Chemical Communications 53, no. 17 (2017): 2563–66. http://dx.doi.org/10.1039/c6cc09743j.

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23

Ravula, Thirupathi, Bikash R. Sahoo, Xiaofeng Dai, and Ayyalusamy Ramamoorthy. "Natural-abundance 17O NMR spectroscopy of magnetically aligned lipid nanodiscs." Chemical Communications 56, no. 69 (2020): 9998–10001. http://dx.doi.org/10.1039/d0cc04011h.

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24

SANDERS, LORI K., WILLIAM D. ARNOLD, and ERIC OLDFIELD. "NMR, IR, Mössbauer and quantum chemical investigations of metalloporphyrins and metalloproteins." Journal of Porphyrins and Phthalocyanines 05, no. 03 (March 2001): 323–33. http://dx.doi.org/10.1002/jpp.319.

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We review contributions made towards the elucidation of CO and O 2 binding geometries in respiratory proteins. Nuclear magnetic resonance, infrared spectroscopy, Mössbauer spectroscopy, X-ray crystallography and quantum chemistry have all been used to investigate the Fe –ligand interactions. Early experimental results showed linear correlations between 17 O chemical shifts and the infrared stretching frequency (νCO) of the CO ligand in carbonmonoxyheme proteins and between the 17 O chemical shift and the 13CO shift. These correlations led to early theoretical investigations of the vibrational frequency of carbon monoxide and of the 13 C and 17 O NMR chemical shifts in the presence of uniform and non-uniform electric fields. Early success in modeling these spectroscopic observables then led to the use of computational methods, in conjunction with experiment, to evaluate ligand-binding geometries in heme proteins. Density functional theory results are described which predict 57 Fe chemical shifts and Mössbauer electric field gradient tensors, 17 O NMR isotropic chemical shifts, chemical shift tensors and nuclear quadrupole coupling constants (e2qQ/h) as well as 13 C isotropic chemical shifts and chemical shift tensors in organometallic clusters, heme model metalloporphyrins and in metalloproteins. A principal result is that CO in most heme proteins has an essentially linear and untilted geometry (τ = 4 °, β = 7 °) which is in extremely good agreement with a recently published X-ray synchrotron structure. CO / O 2 discrimination is thus attributable to polar interactions with the distal histidine residue, rather than major Fe–C–O geometric distortions.

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25

Sharma, Rupali, Jie Zhang, and C. André Ohlin. "Predicting 17O NMR chemical shifts of polyoxometalates using density functional theory." Physical Chemistry Chemical Physics 18, no. 11 (2016): 8235–41. http://dx.doi.org/10.1039/c5cp07766d.

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26

Ehinger, Christian, Christopher P. Gordon, and Christophe Copéret. "Oxygen transfer in electrophilic epoxidation probed by 17O NMR: differentiating between oxidants and role of spectator metal oxo." Chemical Science 10, no. 6 (2019): 1786–95. http://dx.doi.org/10.1039/c8sc04868a.

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27

CLICK, CAROL A., BRIAN R. CHERRY, TODD M. ALAM, and RICHARD K. BROW. "¹⁷ O MAS NMR INVESTIGATION OF P₂O₅ CRYSTALS AND GLASSES." Phosphorus Research Bulletin 13 (2002): 101–6. http://dx.doi.org/10.3363/prb1992.13.0_101.

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28

Jaworski, Aleksander, Baltzar Stevensson, and Mattias Edén. "Direct 17O NMR experimental evidence for Al–NBO bonds in Si-rich and highly polymerized aluminosilicate glasses." Physical Chemistry Chemical Physics 17, no. 28 (2015): 18269–72. http://dx.doi.org/10.1039/c5cp02985f.

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29

Melchior, Jan-Patrick, and Bernhard Frick. "On the nanosecond proton dynamics in phosphoric acid–benzimidazole and phosphoric acid–water mixtures." Physical Chemistry Chemical Physics 19, no. 42 (2017): 28540–54. http://dx.doi.org/10.1039/c7cp04116k.

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Combining ¹H-NMR, ¹⁷O-NMR, and high-resolution backscattering QENS hydrodynamic and structural proton transport in phosphoric acid is separated. The rate limiting steps for structural proton diffusion in mixtures of acid with Brønsted bases are found to occur below the nanosecond timescale.

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30

Makulski, Włodzimierz. "Deuterium isotope effects on 17O nuclear shielding in a single water molecule from NMR gas phase measurements." Physical Chemistry Chemical Physics 22, no. 32 (2020): 17777–80. http://dx.doi.org/10.1039/d0cp03085f.

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The ¹⁷O NMR shielding constants of the isolated molecules: H₂O, HOD and D₂O were measured in the gas phase; the isotope effects were established and small nonadditivity was stated.

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31

Ruggeri, Irene, Andrea La Monaca, Francesca De Giorgio, Francesca Soavi, Catia Arbizzani, Vittorio Berbenni, Chiara Ferrara, and Piercarlo Mustarelli. "Correlating Structure and Properties of Super‐Concentrated Electrolyte Solutions: 17 O NMR and Electrochemical Characterization." ChemElectroChem 6, no. 15 (August 2019): 4002–9. http://dx.doi.org/10.1002/celc.201900829.

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32

Métro, Thomas-Xavier, Christel Gervais, Anthony Martinez, Christian Bonhomme, and Danielle Laurencin. "Innentitelbild: Unleashing the Potential of 17 O NMR Spectroscopy Using Mechanochemistry (Angew. Chem. 24/2017)." Angewandte Chemie 129, no. 24 (May 15, 2017): 6780. http://dx.doi.org/10.1002/ange.201703991.

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33

Seliger, Janez, Janez Plavec, Primož Šket, Veselko Žagar, and Robert Blinc. "17 O NQR and 13 C NMR study of hydrogen-bonded organic ferroelectric croconic acid." physica status solidi (b) 248, no. 9 (May 5, 2011): 2091–96. http://dx.doi.org/10.1002/pssb.201046649.

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34

Grekov, D., Y. Bouhoute, I. Del Rosal, L. Maron, M. Taoufik, R. M. Gauvin, and L. Delevoye. "17O MAS NMR studies of oxo-based olefin metathesis catalysts: a critical assessment of signal enhancement methods." Physical Chemistry Chemical Physics 18, no. 40 (2016): 28157–63. http://dx.doi.org/10.1039/c6cp04667c.

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35

Rowlands, Lucy J., Adam Marks, John M. Sanderson, and Robert V. Law. "17O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers." Chemical Communications 56, no. 92 (2020): 14499–502. http://dx.doi.org/10.1039/d0cc05466f.

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36

Rainer, Daniel N., Cameron M. Rice, Stewart J. Warrender, Sharon E. Ashbrook, and Russell E. Morris. "Mechanochemically assisted hydrolysis in the ADOR process." Chemical Science 11, no. 27 (2020): 7060–69. http://dx.doi.org/10.1039/d0sc02547j.

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37

Li, Wenzheng, Qiang Wang, Jun Xu, Fabien Aussenac, Guodong Qi, Xingling Zhao, Pan Gao, Chao Wang, and Feng Deng. "Probing the surface of γ-Al2O3 by oxygen-17 dynamic nuclear polarization enhanced solid-state NMR spectroscopy." Physical Chemistry Chemical Physics 20, no. 25 (2018): 17218–25. http://dx.doi.org/10.1039/c8cp03132k.

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Different (sub-)surface oxygen species of γ-Al₂O₃ are rapidly detected and differentiated by ¹⁷O dynamic nuclear polarization (DNP) surface enhanced solid state NMR spectroscopy.

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38

Zanonato, Pier Luigi, Zoltán Szabó, Valerie Vallet, Plinio Di Bernardo, and Ingmar Grenthe. "Alkali–metal ion coordination in uranyl(vi) poly-peroxo complexes in solution, inorganic analogues to crown-ethers. Part 2. Complex formation in the tetramethyl ammonium-, Li+-, Na+- and K+-uranyl(vi)–peroxide–carbonate systems." Dalton Transactions 44, no. 37 (2015): 16565–72. http://dx.doi.org/10.1039/c5dt01710f.

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39

Falsone, Gioacchino, Herbert Budzikiewicz, and Detlef Wendisch. "Über Inhaltsstoffe von Euphorbiaceae, 9. Mitt. [1]. Neue Cerebroside aus Euphorbia biglandulosa Desf. / Constituents of Euphorbiaceae, 9. Comm. [1]. New Cerebrosides from Euphorbia biglandulosa Desf." Zeitschrift für Naturforschung B 42, no. 11 (November 1, 1987): 1476–80. http://dx.doi.org/10.1515/znb-1987-1118.

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From the latex of Euphorbia biglandulosa Desf. the cerebrosides 1-O-β-D-glucopyranosyl- 2-N-2′-hydroxy-cis-15-tetracosenoyl-4-hydroxy-eicosasphinga-as-10-enine (1), 1-O-β-D-glucopyranosyl- 2-N-2′-hydroxy-cis-17-hexacosenoyl-4-hydroxy-eicosasphinga-cis-10-enine (2) and 1-O-β-D-glucopyranosyl-2-N-2′-hydroxy-4-hydroxy-eicosasphinga-cis-10-enine (3) were isolated. Structures have been elucidated by 1H NMR , 13C NMR . MS spectroscopy, hydrolysis, and ozonolysis, too.

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40

Hope, Michael A., David M. Halat, Pieter C. M. M. Magusin, Subhradip Paul, Luming Peng, and Clare P. Grey. "Surface-selective direct 17O DNP NMR of CeO2 nanoparticles." Chemical Communications 53, no. 13 (2017): 2142–45. http://dx.doi.org/10.1039/c6cc10145c.

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41

Fernandes, Arantxa, Robert F. Moran, Scott Sneddon, Daniel M. Dawson, David McKay, Giulia P. M. Bignami, Frédéric Blanc, Karl R. Whittle, and Sharon E. Ashbrook. "17O solid-state NMR spectroscopy of A2B2O7 oxides: quantitative isotopic enrichment and spectral acquisition?" RSC Advances 8, no. 13 (2018): 7089–101. http://dx.doi.org/10.1039/c8ra00596f.

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42

Rui-Hua, Li, Jiang Zhan-Peng, Yang Hong-Wei, and Guan Yun-Tao. "Effects of Ions on Chemical Shift of ¹⁷O-NMR(δ(H₂¹⁷O)) and Water Structure." Acta Physico-Chimica Sinica 20, no. 01 (2004): 98–102. http://dx.doi.org/10.3866/pku.whxb20040121.

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43

Zhu, Xingyu, and Yin Gao. "17O NMR spectroscopy-assisted in vitro bioactivity studies of the intermediates formed via Na2S and RSNO cross-linking reactions." RSC Advances 10, no. 65 (2020): 39617–26. http://dx.doi.org/10.1039/d0ra05054g.

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By using UV-Vis, ¹⁵N NMR and ¹⁷O NMR spectroscopy techniques, we characterized the intermediates (SSNO⁻ and SNO⁻) obtained from RSNO and Na₂S cross-linking reaction. We found that SSNO⁻ could serve as NO reservoir in cell culture experiments.

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44

Bignami, Giulia P. M., Zachary H. Davis, Daniel M. Dawson, Samuel A. Morris, Samantha E. Russell, David McKay, Richard E. Parke, Dinu Iuga, Russell E. Morris, and Sharon E. Ashbrook. "Cost-effective 17O enrichment and NMR spectroscopy of mixed-metal terephthalate metal–organic frameworks." Chemical Science 9, no. 4 (2018): 850–59. http://dx.doi.org/10.1039/c7sc04649a.

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45

Perras, Frédéric A., Zhuoran Wang, Pranjali Naik, Igor I. Slowing, and Marek Pruski. "Natural Abundance 17 O DNP NMR Provides Precise O−H Distances and Insights into the Brønsted Acidity of Heterogeneous Catalysts." Angewandte Chemie International Edition 56, no. 31 (June 6, 2017): 9165–69. http://dx.doi.org/10.1002/anie.201704032.

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46

Perras, Frédéric A., Zhuoran Wang, Pranjali Naik, Igor I. Slowing, and Marek Pruski. "Natural Abundance 17 O DNP NMR Provides Precise O−H Distances and Insights into the Brønsted Acidity of Heterogeneous Catalysts." Angewandte Chemie 129, no. 31 (June 6, 2017): 9293–97. http://dx.doi.org/10.1002/ange.201704032.

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47

Makulski, Włodzimierz, Marcin Wilczek, and Karol Jackowski. "17O and 1H NMR spectral parameters in isolated water molecules." Physical Chemistry Chemical Physics 20, no. 35 (2018): 22468–76. http://dx.doi.org/10.1039/c8cp01748d.

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48

Lin, Zhongjie, Julian R. Jones, John V. Hanna, and Mark E. Smith. "A multinuclear solid state NMR spectroscopic study of the structural evolution of disordered calcium silicate sol–gel biomaterials." Physical Chemistry Chemical Physics 17, no. 4 (2015): 2540–49. http://dx.doi.org/10.1039/c4cp04492d.

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Multinuclear solid state NMR, especially ¹⁷O, shows the structural evolution of calcium silicate sol–gel bioactive glasses during stabilisation and subsequent reaction with simulated body fluid.

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49

Fusaro, Luca. "An 17 O NMR study of diamagnetic and paramagnetic lanthanide-tris(oxydiacetate) complexes in aqueous solution." Magnetic Resonance in Chemistry 56, no. 12 (August 7, 2018): 1168–75. http://dx.doi.org/10.1002/mrc.4781.

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50

Yamada, Shinji, Nodoka Sako, Kazuhiko Yamada, Kenzo Deguchi, and Tadashi Shimizu. "Porous organic hydrate crystals: structure and dynamic behaviour of water clusters." CrystEngComm 17, no. 30 (2015): 5629–33. http://dx.doi.org/10.1039/c4ce02517b.

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Infinite water clusters with a T5(2) motif were observed in porous crystals of 4-nitrostyrylpyridine hydrochloride, the behavior of which was revealed by solid-state ¹⁷O NMR spectroscopic analyses.

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