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Journal articles on the topic '2-(2' -hydroxyphenyl)benzoxazole'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Syetov, Y. "Computational study of nonlinear optical properties of benzoxazoles exhibiting excited state proton transfer." Journal of Physics and Electronics 27, no. 1 (2019): 47–50. http://dx.doi.org/10.15421/331908.

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Hyperpolarizability of molecules of 2-(2'-hydroxyphenyl)benzoxazole and 2,5-bis(2-benzoxazolyl)phenol is calculated by density functional theory quadratic response method for static electric field and hyper-Rayleigh scattering at 532 nm. It is found that 2,5-bis(2-benzoxazolyl)phenol demonstrates the hyperpolarizability about ten times larger than 2-(2'-hydroxyphenyl)benzoxazole. Dominant component of the hyperpolarizability tensor corresponds to the long axis of the molecule.

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2

XIAO, DONG, GUILAN ZHANG, HAIYAN WANG, GUOQING TANG, and WENJU CHEN. "INVESTIGATION ON NONLINEAR TRANSMISSION PROPERTY OF EXCITED STATE PROTON TRANSFER MOLECULE 2-(2′-HYDROXYPHENYL)BENZOXAZOLE." Journal of Nonlinear Optical Physics & Materials 09, no. 03 (2000): 309–14. http://dx.doi.org/10.1142/s0218863500000248.

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Nonlinear transmission property of excited state proton transfer molecule 2-(2′-hydroxyphenyl)benzoxazole was investigated at 355 nm and 532 nm using picosecond laser pulses. The experiment result shows that the transmissivity of 2-(2′-hydroxyphenyl)benzoxazole is nonlinear at 355 nm but it is linear at 532 nm. The nonlinear transmissivity of 2-(2′-hydroxyphenyl)benzoxazole originates from the larger nonlinearity of tautomer formed in excited state proton transfer process. Therefore 2-(2′-hydroxyphenyl)benzoxazole might be used as ultrafast optical amplitude limit material.

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3

Syetov, Y. "Theoretical modeling of two-photon absorption of benzoxazoles exhibiting excited state proton transfer." Journal of Physics and Electronics 26, no. 2 (2018): 55–58. http://dx.doi.org/10.15421/331824.

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Two-photon absorption spectra of 2-(2'-hydroxyphenyl)benzoxazole, 2,5-bis(2-benzoxazolyl)phenol and 2,5-bis(2-benzoxazolyl)hydroquinone are modeled by time-dependent density functional theory calculations. In contrast to the linear absorption, where the transitions to the two lowest excited states are leading, the two-photon absorption cross sections are significant for the transitions to higher states which are weak in one-photon absorption spectra. The 2,5-bis(2-benzoxazolyl)phenol and 2,5-bis(2-benzoxazolyl)hydroquinone demonstrate the maximum cross section of about ten times larger than th

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4

Tong, Yi-Ping. "2-(2-Hydroxyphenyl)-1,3-benzoxazole." Acta Crystallographica Section E Structure Reports Online 61, no. 9 (2005): o3076—o3078. http://dx.doi.org/10.1107/s1600536805027066.

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5

Danilenko, Nadezhda V., Mariia O. Lutsuk, and Andrei I. Khlebnikov. "4-(Benzoxazol-2-yl)phenyl 3-((3-Chloro-1,4-Naphthoquinon-2-yl)amino)phenyl Sulfate." Molbank 2024, no. 4 (2024): M1930. https://doi.org/10.3390/m1930.

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New 4-(benzoxazol-2-yl)phenyl 3-((3-chloro-1,4-naphthoquinon-2-yl)amino)phenyl sulfate was synthesized via the SuFEx click reaction between fluorosulfate-containing 1,4-naphthoquinone and 2-(4-hydroxyphenyl)benzoxazole. 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) was used as an organic base, while triethylamine was inactive in this reaction.

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6

Kwak, Min-Jung, and Young-Mi Kim. "Photostable BF2-Chelated Fluorophores Based on 2-(2'-Hydroxyphenyl)benzoxazole and 2-(2'-Hydroxyphenyl)benzothiazole." Bulletin of the Korean Chemical Society 30, no. 12 (2009): 2865–66. http://dx.doi.org/10.5012/bkcs.2009.30.12.2865.

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7

Tang, Zhe, Haiyun Han, Junxia Ding, and Panwang Zhou. "Dual fluorescence of 2-(2′-hydroxyphenyl) benzoxazole derivatives via the branched decays from the upper excited-state." Physical Chemistry Chemical Physics 23, no. 48 (2021): 27304–11. http://dx.doi.org/10.1039/d1cp03546k.

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8

Abou-Zied, Osama K., Ralph Jimenez, Elizabeth H. Z. Thompson, David P. Millar, and Floyd E. Romesberg. "Solvent-Dependent Photoinduced Tautomerization of 2-(2‘-Hydroxyphenyl)benzoxazole." Journal of Physical Chemistry A 106, no. 15 (2002): 3665–72. http://dx.doi.org/10.1021/jp013915o.

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9

Dey, Joy Krishna, and Sneh K. Dogra. "Solvatochromism and prototropism of 2-(3′-hydroxyphenyl)benzoxazole and 2-(4′-hydroxyphenyl)benzoxazole in the excited singlet state." Journal of Photochemistry and Photobiology A: Chemistry 59, no. 3 (1991): 307–21. http://dx.doi.org/10.1016/1010-6030(91)87083-8.

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10

Syetov, Y. A., and V. M. Moiseyenko. "Computational study of electronic-vibrational spectrum of rotamers of 2-(2'-hydroxyphenyl)benzoxazole." Journal of Physics and Electronics 30, no. 2 (2022): 63–66. http://dx.doi.org/10.15421/332221.

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UV-vis absorption spectrum of internally hydrogen-bonded enol structures of 2-(2'-hydroxyphenyl)benzoxazole is calculated for the transitions to the first excited state using the Franck-Condon approximation and harmonic model for vibrations. It is shown that the absorption spectrum of the structure with the hydrogen bond OH...O is shifted to larger energy by about 0.13 eV compared to the spectrum of the most stable structure with the hydrogen bond OH...N. The largest intensity of vibronic transitions to the first electronic state of the OH...O structure demonstrates high-frequency vibrations i

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11

Suman, Verma, and Seth Gita. "Potentiometric studies on the complexes of Cu(II) and Ni(II) with some amino acids and 2-(2' -hydroxyphenyl) benzoxazole." Journal of Indian Chemical Society Vol. 88, Sep 2011 (2011): 1435–38. https://doi.org/10.5281/zenodo.5790393.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004, Rajasthan, India <em>E-mail</em> : gita_seth@yahoo.co.in <em>Manuscript received 30 December 2009, revised 27 January 2011. accepted 02 February 2011</em> The stability constants of binary and ternary metal complexes of copper(ll) and nickel (ll) with some amino acids (L-Ieucine, L-valine, I.-serine and I.-isoleucine) as primary ligands and 2-(2'-hydroxyphenyl)benzoxazole (HBO) as secondary ligand have been determined potentiometrically at an ionic strength 1.0 mol dm-3 KN03 at 35 ± 1°C. The stability of the binar

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12

Massue, Julien, Pascal Retailleau, Gilles Ulrich, and Raymond Ziessel. "Synthesis of luminescent BPh2-coordinated 2-(2′-hydroxyphenyl)benzoxazole (HBO)." New Journal of Chemistry 37, no. 4 (2013): 1224. http://dx.doi.org/10.1039/c3nj41052h.

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13

Li, Xiaochuan, Yajuan Li, Junna Zhang, and Young-A. Son. "Crystal structure of 2-(4-diethylamino-2-hydroxyphenyl)-benzoxazole, C17H18N2O2." Zeitschrift für Kristallographie - New Crystal Structures 228, no. 1 (2013): 99–100. http://dx.doi.org/10.1524/ncrs.2013.0063.

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14

Massue, Julien, Denis Frath, Gilles Ulrich, Pascal Retailleau, and Raymond Ziessel. "Synthesis of Luminescent 2-(2′-Hydroxyphenyl)benzoxazole (HBO) Borate Complexes." Organic Letters 14, no. 1 (2011): 230–33. http://dx.doi.org/10.1021/ol203014e.

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15

Zhang, G., H. Wang, Y. Yu, F. Xiong, G. Tang, and W. Chen. "Optical switching of 2-(2′-hydroxyphenyl) benzoxazole in different solvents." Applied Physics B 76, no. 6 (2003): 677–81. http://dx.doi.org/10.1007/s00340-003-1164-0.

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16

Syetov, Y. "Luminescence spectrum of 2-(2'-hydroxyphenyl)benzoxazole in the solid state." Ukrainian Journal of Physical Optics 14, no. 1 (2013): 1. http://dx.doi.org/10.3116/16091833/14/1/1/2013.

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17

Meisner, Quinton J., Ali H. Younes, Zhao Yuan, Kesavapillai Sreenath, Joseph J. M. Hurley, and Lei Zhu. "Excitation-Dependent Multiple Fluorescence of a Substituted 2-(2′-Hydroxyphenyl)benzoxazole." Journal of Physical Chemistry A 122, no. 47 (2018): 9209–23. http://dx.doi.org/10.1021/acs.jpca.8b07988.

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18

Yang, G., Z. A. Dreger, Y. Li, and H. G. Drickamer. "Pressure-Induced Isomerization of 2-(2‘-Hydroxyphenyl)benzoxazole in Solid Media." Journal of Physical Chemistry A 101, no. 43 (1997): 7948–52. http://dx.doi.org/10.1021/jp971566l.

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19

ZHANG, GUILAN, FEIBING XIONG, BAO ZHANG, et al. "EFFECT OF SOLVENT ON NONLINEAR REFRACTIVE INDEX OF 2-(2′-HYDROXYPHENYL) BENZOXAZOLE." Journal of Nonlinear Optical Physics & Materials 12, no. 03 (2003): 385–91. http://dx.doi.org/10.1142/s0218863503001511.

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Nonlinear refractive indexes n2 of 2-(2′-hydroxyphenyl) benzoxazole (HBO) in three species of solvent (cyclohexane, ethanol and dimethyl sulfoxide) have been determined by using the Z-scan technique. The experimental results show that the n2 of HBO is strongly dependent on the polarity of the solvent. Through the study on the absorption and fluorescence spectra of HBO in different solvents, we regard that the principal origin of the nonlinear refractive index of HBO is not the thermal effect because of absorption of incident light but the excited state intramolecular proton transfer of HBO und

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20

Lavtchieva, L., V. Enchev, and Z. Smedarchina. "Golden rule study of excited-state proton transfer in 2-(2-hydroxyphenyl)benzoxazole and 2-(2-hydroxy-4-methylphenyl)benzoxazole." Journal of Physical Chemistry 97, no. 2 (1993): 306–10. http://dx.doi.org/10.1021/j100104a009.

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21

Zahid, N. Idayu, Osama K. Abou-Zied, N. A. Nabila Saari та Rauzah Hashim. "Comparative study of the inverse versus normal bicontinuous cubic phases of the β-d-glucopyranoside water-driven self-assemblies using fluorescent probes". RSC Advances 6, № 1 (2016): 227–35. http://dx.doi.org/10.1039/c5ra19794e.

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This work investigates the head group region of the inverse and normal bicontinuous cubic phases (Ia3d space group) of the glucopyranoside/water system using 2-(2′-hydroxyphenyl)benzoxazole and its derivatives as fluorescent probes.

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22

Li, Changming, Wei Guo, Panwang Zhou, and Zhe Tang. "The effects of the heteroatom and position on excited-state intramolecular proton transfer of new hydroxyphenyl benzoxazole derivatives: a time-dependent density functional theory study." Organic Chemistry Frontiers 6, no. 11 (2019): 1807–15. http://dx.doi.org/10.1039/c9qo00295b.

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The effects of the heteroatom and position on excited-state intramolecular proton transfer (ESIPT) of 2-[4′-(N-4,6-dichloro-1,3,5-triazi-n-2-yl)2′hydroxyphenyl]benzoxazole (4THBO) have been investigated via time-dependent density functional theory studies.

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23

Syetov, Y. "Theoretical modeling of defects in the molecular crystal of 2-(2'-hydroxyphenyl)benzothiazole." Journal of Physics and Electronics 28, no. 1 (2020): 43–48. http://dx.doi.org/10.15421/332008.

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2-(2'-hydroxyphenyl)benzothiazole is a photoreactive compound that exhibits excited state intramolecular proton transfer in the structure with an OH...N hydrogen bond. Energy of various structures is calculated for isolated molecules, clusters and periodic structures of 2-(2'-hydroxyphenyl)benzothiazole by density-functional based tight-binding methods. It is shown that the most stable conformation of the isolated molecule is a planar structure with an OH...N hydrogen bond. Other conformations have significantly larger energy in comparison with the average room temperature heat energy that imp

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24

Ikegami, Masashi, and Tatsuo Arai. "Photoinduced intramolecular hydrogen atom transfer in 2-(2-hydroxyphenyl)benzoxazole and 2-(2-hydroxyphenyl)benzothiazole studied by laser flash photolysis." Journal of the Chemical Society, Perkin Transactions 2, no. 7 (May 14, 2002): 1296–301. http://dx.doi.org/10.1039/b202559k.

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25

Qin, Wei, Sherine O. Obare, Catherine J. Murphy, and S. Michael Angel. "Specific fluorescence determination of lithium ion based on 2-(2-hydroxyphenyl)benzoxazole." Analyst 126, no. 9 (2001): 1499–501. http://dx.doi.org/10.1039/b104216p.

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26

Kim, Won Sam, Jung Min You, Burm-Jong Lee, Yoon-Ki Jang, Dong-Eun Kim, and Young-Soo Kwon. "Synthesis and blue electroluminescent properties of zinc (II) [2-(2-hydroxyphenyl)benzoxazole]." Thin Solid Films 515, no. 12 (2007): 5070–74. http://dx.doi.org/10.1016/j.tsf.2006.10.070.

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27

Yang, Guoqiang, Fabrice Morlet-Savary, Zhaokui Peng, Shikang Wu, and Jean-Pierre Fouassier. "Triplet-triplet absorption of 2-(2′-hydroxyphenyl) benzoxazole (HBO) in polar solvents." Chemical Physics Letters 256, no. 4-5 (1996): 536–42. http://dx.doi.org/10.1016/0009-2614(96)00463-0.

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28

Krishnamurthy, Mannam, and Sneh K. Dogra. "Proton transfer of 2-(2′-hydroxyphenyl)benzoxazole in the excited singlet state." Journal of Photochemistry 32, no. 2 (1986): 235–42. http://dx.doi.org/10.1016/0047-2670(86)87011-3.

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29

Tanaka, Kiyoshi, Makoto Deguchi, Satoru Yamaguchi, Kouji Yamada, and Satoru Iwata. "Solvent- and concentration-sensitive fluorescence of 2-(3,4,5,6-tetrafluoro-2-hydroxyphenyl)benzoxazole." Journal of Heterocyclic Chemistry 38, no. 1 (2001): 131–36. http://dx.doi.org/10.1002/jhet.5570380118.

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30

P., Madhava Reddy, Venkata Ramana Reddy Ch., and Satyanarayana B. "Equilibrium studies on ternary chelates of trivalent metal ions with 2-(2-hydroxyphenyl)benzimidazole, 2-(2-hydroxyphenyl)benzoxazole and other ligands in solution." Journal of Indian Chemical Society Vol. 83, Jul 2006 (2006): 722–24. https://doi.org/10.5281/zenodo.5825182.

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Department of Chemistry, University College of Engineering, Osmania University, Hyderabad-500 007, India Department of Chemistry, Chaitanya Bharathi Institute of Technology, Gandipet, Hyderabad-500 075, India <em>E-mail</em>: vrr9@yahoo.com <em>Manuscript received 21 December 2005, accepted 24 April 2006</em> The pHh-matric equilibrium studies of (1 : 1 : 1) ternary cheIales,MAL where, M=La<sup>III</sup>,Pr<sup>III,</sup>Nd<sup>III</sup>, Gd<sup>III</sup> , DY<sup>III</sup> and Y<sup>III</sup>;L = 2-(2-hydroxypltenyl)benzimidazole and 2-(2-hydroxyphenyl)benzoxazole and A = imlnodlacetic acid a

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31

Itoh, Michiya, and Yoshihisa Fujiwara. "Transient absorption and two-step laser excitation fluorescence studies of photoisomerization in 2-(2-hydroxyphenyl)benzoxazole and 2-(2-hydroxyphenyl)benzothiazole." Journal of the American Chemical Society 107, no. 6 (1985): 1561–65. http://dx.doi.org/10.1021/ja00292a018.

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32

Syetov, Y. A., A. O. Diachenko, V. S. Mukharovska, and V. M. Moiseyenko. "Calculations of molecular properties of 2-(2'-hydroxyphenyl)benzoxazole by semi-empirical tight-binding methods." Journal of Physics and Electronics 30, no. 1 (2022): 53–56. http://dx.doi.org/10.15421/332208.

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The semi-empirical tight-binding methods GFN1-xTB and GFN2-xTB are applied to calculations of structure, energy and normal vibrations of the molecule of 2-(2'-hydroxyphenyl)benzoxazole undergoing excited state intramolecular proton transfer. The results are compared with ones obtained by the density-functional tight-binding methods with hydrogen interaction corrections and density functional theory. The GFN2-xTB method is found to provide good correspondence to the results obtained by more accurate but much slower density functional theory method for geometrical parameters of hydrogen bond, re

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33

LAVTCHIEVA, L., V. ENCHEV, and Z. SMEDARCHINA. "ChemInform Abstract: Golden Rule Study of Excited-State Proton Transfer in 2-(2′- Hydroxyphenyl)benzoxazole and 2-(2′-Hydroxy-4′-methylphenyl) benzoxazole." ChemInform 24, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199318055.

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34

Purkayastha, Pradipta, and Nitin Chattopadhyay. "Role of rotamerisation and excited state intramolecular proton transfer in the photophysics of 2-(2′-hydroxyphenyl)benzoxazole, 2-(2′-hydroxyphenyl)benzimidazole and 2-(2′-hydroxyphenyl)benzothiazole: a theoretical study." Physical Chemistry Chemical Physics 2, no. 2 (2000): 203–10. http://dx.doi.org/10.1039/a908359f.

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35

Sun, Simei, Song Zhang, Jiao Song, et al. "Ultrafast proton transfer dynamics of 2-(2′-hydroxyphenyl)benzoxazole dye in different solvents." Chinese Physics B 31, no. 2 (2022): 027803. http://dx.doi.org/10.1088/1674-1056/ac3734.

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The excited-state intramolecular proton transfer of 2-(2′-hydroxyphenyl)benzoxazole dye in different solvents is investigated using ultrafast femtosecond transient absorption spectroscopy combined with quantum chemical calculations. Conformational conversion from the syn-enol configuration to the keto configuration is proposed as the mechanism of excited-state intramolecular proton transfer. The duration of excited-state intramolecular proton transfer is measured to range from 50 fs to 200 fs in different solvents. This time is strongly dependent on the calculated energy gap between the N-S0 a

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36

Nagaoka, Shinichi, Akinori Itoh, Kazuo Mukai, and Umpei Nagashima. "Investigation of triplet states of 2-(2-hydroxyphenyl)benzothiazole and 2-(2-hydroxyphenyl)benzoxazole by transient absorption spectroscopy and ab initio calculations." Journal of Physical Chemistry 97, no. 44 (1993): 11385–92. http://dx.doi.org/10.1021/j100146a008.

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37

Kim, Tae Hyeon, Na Young Kwon, Ji Hye Son, Changduk Yang, Minjung Lee, and Taek Seung Lee. "Self-Assembly of Supramolecualr Metallogelator Containing 2-(2′-Hydroxyphenyl) benzoxazole/Zn(II) Chelate." Journal of Nanoscience and Nanotechnology 10, no. 10 (2010): 6929–33. http://dx.doi.org/10.1166/jnn.2010.2972.

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38

Yuan, Zhao, Qing Tang, Kesavapillai Sreenath, et al. "Absorption and Emission Sensitivity of 2-(2′-Hydroxyphenyl)benzoxazole to Solvents and Impurities." Photochemistry and Photobiology 91, no. 3 (2014): 586–98. http://dx.doi.org/10.1111/php.12393.

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39

Kocher, Christoph, Paul Smith, and Christoph Weder. "Aromatic 2-(2′-hydroxyphenyl)benzoxazole esters: a novel class of caged photoluminescent dyes." J. Mater. Chem. 12, no. 9 (2002): 2620–26. http://dx.doi.org/10.1039/b202719b.

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40

Chen, Wei-Hua, and Yi Pang. "Efficient synthesis of 2-(2′-hydroxyphenyl)benzoxazole by palladium(II)-catalyzed oxidative cyclization." Tetrahedron Letters 50, no. 48 (2009): 6680–83. http://dx.doi.org/10.1016/j.tetlet.2009.09.084.

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41

Vetrova, E. V., I. O. Tupaeva, V. I. Minkin, and A. V. Metelitsa. "Chromogenic and Fluorescent Properties of 2-(2-Carboethoxy-3,4-Dichloro-6-Hydroxyphenyl)Benzoxazole." High Energy Chemistry 57, S3 (2023): S488—S493. http://dx.doi.org/10.1134/s0018143923090199.

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42

Ikegami, Masashi, and Tatsuo Arai. "Laser Flash Photolysis Study on Hydrogen Atom Transfer of 2-(2-Hydroxyphenyl)benzoxazole and 2-(2-Hydroxyphenyl)benzothiazole in the Triplet Excited State." Chemistry Letters 29, no. 9 (2000): 996–97. http://dx.doi.org/10.1246/cl.2000.996.

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43

Mordzinski, A., and K. H. Grellmann. "Excited-state proton-transfer reactions in 2-(2'-hydroxyphenyl)benzoxazole. Role of triplet states." Journal of Physical Chemistry 90, no. 22 (1986): 5503–6. http://dx.doi.org/10.1021/j100280a006.

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44

López-Ruiz, Heraclio, Horacio Briseño-Ortega, Susana Rojas-Lima, Rosa Santillan, and Norberto Farfán. "Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives." Tetrahedron Letters 52, no. 33 (2011): 4308–12. http://dx.doi.org/10.1016/j.tetlet.2011.06.039.

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45

Rodembusch, Fabiano Severo, Fernanda Raquel Brand, Dione Silva Corrêa, João Claudio Pocos, Marcia Martinelli, and Valter Stefani. "Transition metal complexes from 2-(2′-hydroxyphenyl)benzoxazole: A spectroscopic and thermogravimetric stability study." Materials Chemistry and Physics 92, no. 2-3 (2005): 389–93. http://dx.doi.org/10.1016/j.matchemphys.2005.01.049.

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46

Massue, Julien, Gilles Ulrich, Filippo Monti, and Andrea Barbieri. "Phosphorescent Cyclometalated Iridium(III) Complexes Bearing Ethynyl-Extended 2-(2'-Hydroxyphenyl) Benzoxazole Ancillary Ligands." European Journal of Inorganic Chemistry 2020, no. 18 (2020): 1775–82. http://dx.doi.org/10.1002/ejic.202000114.

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47

NAGAOKA, S., A. ITOH, K. MUKAI, and U. NAGASHIMA. "ChemInform Abstract: Investigation of Triplet States of 2-(2′-Hydroxyphenyl)benzothiazole and 2-(2′-Hydroxyphenyl)benzoxazole by Transient Absorption Spectroscopy and ab initio Calculations." ChemInform 25, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199406040.

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48

Muto, Masahiro, Kousuke Morinaga, Momoko Nishihashi, Yasunori Yamada, and Masayuki Koikawa. "Structural and Magnetic Properties of Dimeric Capsule Assemblies Formed by Cyclic Trinuclear Complexes." Molecules 29, no. 18 (2024): 4307. http://dx.doi.org/10.3390/molecules29184307.

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Cyclic trinuclear homo-metal complexes, [{Fe(L3+2Br)py}3] (1) and [{Mn(L3+2Br)}3(py)2 MeOH] (2), along with a hetero-metal complex, [FeMn2(L3+2H)3(DMF)3] (3), were synthesized using asymmetric ditopic ligands (H3L3+2H: 2-(2-hydroxyphenyl)-6-ol-5-(salicylideneamino)benzoxazole, H3L3+2Br: 2-(2-hydrox-5-bromoyphenyl)-6-ol-5-(5-bromosalicylideneamino)benzoxazole). The molecular structure of 1 is characterized by a tripod structure with three-fold symmetry, where an enantiomer pair forms a dimeric capsule with dimensions of approximately 3 × 1.6 × 1.6 nm3. Complexes 2 and 3, which lack three-fold s

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49

Valdés, Hugo, Reyna Reyes-Martínez, J. Roberto Pioquinto-Mendoza, et al. "Reactivity of 2-(2-hydroxyphenyl)benzoxazole and 2-(2-hydroxyphenyl)benzothiazole towards group 10 transition metals. Evaluation in palladium catalyzed Suzuki–Miyaura C–C couplings." Inorganica Chimica Acta 431 (May 2015): 222–29. http://dx.doi.org/10.1016/j.ica.2015.03.012.

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50

Rios, M. A., and M. C. Rios. "Ab Initio Study of Ground and Excited State Proton Transfer in 2-(2'-Hydroxyphenyl)benzoxazole." Journal of Physical Chemistry 99, no. 33 (1995): 12456–60. http://dx.doi.org/10.1021/j100033a014.

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