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Journal articles on the topic 'Mercaptobenzoyl'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Kimura, Kunio, and Yuhiko Yamashita. "Synthesis and characterization of poly(4-mercaptobenzoyl) whiskers from S-acetyl-4-mercaptobenzoic acid." Polymer 35, no. 15 (1994): 3311–16. http://dx.doi.org/10.1016/0032-3861(94)90140-6.

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2

Aitken, R. Alan, Alexandra H. Campbell, Chloé E. Fletcher, and Alexandra M. Z. Slawin. "2,2′-Trisulfanediyldibenzoyl Chloride." Molbank 2023, no. 3 (2023): M1731. http://dx.doi.org/10.3390/m1731.

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The X-ray structure of the title compound, formed at low conversion in the reaction of thiosalicylic acid with thionyl chloride, has been determined. The acid chloride groups are oriented to permit an attractive non-bonding O…S interaction. Mechanisms are suggested for the formation of this unexpected product. 1H and 13C NMR data are also reported for the first time for the major reaction product, 2-mercaptobenzoyl chloride.

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3

Kobashi, Kazufumi, Kunio Kimura, and Yuhiko Yamashita. "Polymer Whiskers Composed ofp-Oxybenzoyl andp-Mercaptobenzoyl Having Graded Compositions." Macromolecules 37, no. 20 (2004): 7570–77. http://dx.doi.org/10.1021/ma035962f.

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4

Evans, D. J., D. L. Hughes, G. J. Leigh, G. Garcia, and M. D. Santana. "Structure of 4,7-bis(4-mercaptobenzoyl)-1-tosyl-1,4,7-triazacyclononane." Acta Crystallographica Section C Crystal Structure Communications 49, no. 5 (1993): 905–8. http://dx.doi.org/10.1107/s0108270192012770.

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5

Kobashi, Kazufumi, Kunio Kimura, Tetsuya Uchida, Yuhiko Yamashita, and Kaoru Shimamura. "Polymer whiskers based on p-mercaptobenzoyl and p-oxybenzoyl blocks." Polymer 46, no. 7 (2005): 2191–200. http://dx.doi.org/10.1016/j.polymer.2005.01.016.

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6

Bahde, Robert J., Daniel H. Appella, and William C. Trenkle. "A one-pot preparation of N-2-mercaptobenzoyl-amino amides." Tetrahedron Letters 52, no. 32 (2011): 4103–5. http://dx.doi.org/10.1016/j.tetlet.2011.05.115.

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7

Niu, Qingfen, Hongjian Sun, Lin Wang, Qingping Hu, and Xiaoyan Li. "Reactivity of mer-hydrido(2-mercaptobenzoyl)tris(trimethylphosphine)cobalt(iii) complex." Dalton Transactions 43, no. 10 (2014): 4059. http://dx.doi.org/10.1039/c3dt52519h.

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8

Kimura, Kunio, Daisuke Nakajima, Kazufumi Kobashi, Shin-ichiro Kohama, Tetsuya Uchida, and Yuhiko Yamashita. "Morphology Control of Poly(p-mercaptobenzoyl) by Modification of Oligomer End-group." Polymer Journal 37, no. 7 (2005): 471–79. http://dx.doi.org/10.1295/polymj.37.471.

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9

EVANS, D. J., D. L. HUGHES, G. J. LEIGH, G. GARCIA, and M. D. SANTANA. "ChemInform Abstract: Structure of 4,7-Bis(4-mercaptobenzoyl)-1-tosyl-1,4,7- triazacyclononane." ChemInform 24, no. 43 (2010): no. http://dx.doi.org/10.1002/chin.199343044.

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10

Ershov, А. Yu, I. V. Lagoda, D. G. Nasledov, et al. "Synthesis of (2R,4R)-2-alkyl-3-(2-mercaptobenzoyl)thiazolidine-4-carboxylic acids." Russian Journal of Organic Chemistry 53, no. 11 (2017): 1682–86. http://dx.doi.org/10.1134/s1070428017110124.

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11

Kobashi, Kazufumi, Kunio Kimura, Yuhiko Yamashita, Tetsuya Uchida, and Yoshimitsu Sakaguchi. "Self-Assembling Polycondensation for Preparation of Poly(p-oxybenzoyl-alt-p-mercaptobenzoyl) Whisker." Macromolecules 36, no. 12 (2003): 4268–75. http://dx.doi.org/10.1021/ma030046n.

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12

Frome, Michelle J., Lisa E. Cooper, Breia J. Lewis, Michael J. Ferguson, and Christopher J. A. Daley. "Bis(tetraethylammonium) bis[N-(2-mercaptobenzoyl)-1,3-benzothiazole-2-carboxamidato]cobaltate(III) chloride." Acta Crystallographica Section E Structure Reports Online 62, no. 3 (2006): m555—m557. http://dx.doi.org/10.1107/s1600536806005356.

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13

Pham, Tuan Anh, Jong Su Kim, Don Kim, and Yeon Tae Jeong. "Preparation of Gold Nanoparticles/Graphene Hybrid Using 4-Mercaptobenzoyl Functionalized Graphene Nanosheets as Templates." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 43, no. 1 (2012): 40–45. http://dx.doi.org/10.1080/15533174.2012.682685.

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14

Kimura, Kunio, Daisuke Nakajima, Kazufumi Kobashi, et al. "Whisker of poly(p-oxybenzoyl-co-p-mercaptobenzoyl)?influence of sequence on polymer morphology." Polymers for Advanced Technologies 11, no. 8-12 (2000): 747–56. http://dx.doi.org/10.1002/1099-1581(200008/12)11:8/12<747::aid-pat53>3.0.co;2-4.

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15

Ichimori, Toshimitsu, Shinichi Yamazaki, and Kunio Kimura. "Heterogeneous polycondensation for composition control of poly(p -mercaptobenzoyl-co-p -benzamide) by shearing." Journal of Polymer Science Part A: Polymer Chemistry 51, no. 20 (2013): 4301–8. http://dx.doi.org/10.1002/pola.26839.

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16

Kobashi, Kazufumi, Kunio Kimura, and Yuhiko Yamashita. "Influence of short distance sequence regularity on preparation of poly(p-oxybenzoyl-co-p-mercaptobenzoyl) whisker." Polymer 45, no. 21 (2004): 7099–107. http://dx.doi.org/10.1016/j.polymer.2004.08.017.

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17

Niu, Qingfen, Hongjian Sun, Xiaoyan Li, H. F. Klein, and Ulrich Flörke. "Synthesis and Catalytic Application in Hydrosilylation of the Complexmer-Hydrido(2-mercaptobenzoyl)tris(trimethylphosphine)cobalt(III)." Organometallics 32, no. 18 (2013): 5235–38. http://dx.doi.org/10.1021/om4005687.

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18

Choi, Hyun-Jung, In-Yup Jeon, Dong Wook Chang, et al. "Preparation and Electrocatalytic Activity of Gold Nanoparticles Immobilized on the Surface of 4-Mercaptobenzoyl-Functionalized Multiwalled Carbon Nanotubes." Journal of Physical Chemistry C 115, no. 5 (2010): 1746–51. http://dx.doi.org/10.1021/jp109890u.

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19

Chowdhury, Shubhamoy, Ali Canlier, Nobuyoshi Koshino, and Yasuhisa Ikeda. "Novel oxorhenium(V) ‘3+1’ mixed ligand complexes with 3-thiapentane-1,5-dithiolate and functional mercaptobenzoyl amino acid ethyl ester." Inorganica Chimica Acta 361, no. 1 (2008): 145–52. http://dx.doi.org/10.1016/j.ica.2007.06.038.

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20

Pavan, Mysore S., Sounak Sarkar, and Tayur N. Guru Row. "Exploring the rare S—H...S hydrogen bond using charge density analysis in isomers of mercaptobenzoic acid." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 73, no. 4 (2017): 626–33. http://dx.doi.org/10.1107/s2052520617008344.

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Experimental and theoretical charge density analyses on isomers of mercaptobenzoic acid have been carried out to quantify the hydrogen bonding of the hitherto less explored thiols, to assess the strength of the interactions using the topological features of the electron density. The electron density study offers interesting insights into the nature of the S—H...S interaction. The interaction energy is comparable with that of a weak hydrogen bond. The strength and directionality of the S—H...S hydrogen bond is demonstrated to be mainly due to the conformation locking potential of the intramolec

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21

Cowper, Ben, Tsz Mei Sze, Bhavesh Premdjee, Aileen F. Bongat White, Andrew Hacking, and Derek Macmillan. "Examination of mercaptobenzyl sulfonates as catalysts for native chemical ligation: application to the assembly of a glycosylated Glucagon-Like Peptide 1 (GLP-1) analogue." Chemical Communications 51, no. 15 (2015): 3208–10. http://dx.doi.org/10.1039/c4cc09502b.

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22

Zeyat, Gehad, and Karola Rück-Braun. "Building photoswitchable 3,4'-AMPB peptides: Probing chemical ligation methods with reducible azobenzene thioesters." Beilstein Journal of Organic Chemistry 8 (June 18, 2012): 890–96. http://dx.doi.org/10.3762/bjoc.8.101.

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Photoswitchable peptides were synthesized by using cysteine- and auxiliary-based native chemical ligation reactions. For this purpose, the two regioisomeric azobenzene building blocks 3,4'-AMPB thioester 1b and 4,4'-AMPB thioester 2b were employed in the ligation reactions. While 4,4'-AMPB requires the 4,5,6-trimethoxy-2-mercaptobenzyl auxiliary to minimize reduction of the diazene unit, 3,4'-AMPB can be used in combination with the 4,5,6-trimethoxy-2-mercaptobenzyl auxiliary as well as the N α-2-mercaptoethyl auxiliary. Thus, 3,4'-AMPB derivatives/peptides proved to be significantly less pron

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23

Cianferotti, Claudio, Valentina Faltoni, Elena Cini, et al. "Antibody drug conjugates with hydroxamic acid cargos for histone deacetylase (HDAC) inhibition." Chemical Communications 57, no. 7 (2021): 867–70. http://dx.doi.org/10.1039/d0cc06131j.

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24

Lin, Yi-Jyun, Po-Cheng Chen, Zhiqin Yuan, Jia-Ying Ma, and Huan-Tsung Chang. "The isomeric effect of mercaptobenzoic acids on the preparation and fluorescence properties of copper nanoclusters." Chemical Communications 51, no. 60 (2015): 11983–86. http://dx.doi.org/10.1039/c5cc02342d.

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25

Fritz, Thorsten, Gunther Steinfeld, and Berthold Kersting. "Preparation and Characterization of Mononuclear Ni Complexes of Tetradentate Amine-thioether and Amine-thiolate Ligands." Zeitschrift für Naturforschung B 62, no. 4 (2007): 508–18. http://dx.doi.org/10.1515/znb-2007-0404.

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A short route for the preparation of tetradentate amine-thioether and amine-thiolate ligands derived from thiosalen is reported. The ligating properties of several of the synthesized ligands towards Ni(II) has been examined. The diamine-dithiophenolate ligands (L6)2− [H2L6 = N,N′-dimethyl-N,N;-di(2- mercaptobenzyl)-ethane-1,2-diamine] and (L7)2− [H2L7 = N,N′-di(2-mercaptobenzyl)-piperazine] support the formation of four-coordinate NiIIN2S2 complexes [NiII(L6)] (10) and [NiII(L7)] (11). By contrast, the amine-thioethers 2 [N′,N″-bis(2-(tert-butylthio)benzyl)ethane-1,2-diamine], L2 [8,11- diaza-

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26

Kong, Chuncai, Jian Lv, Shaodong Sun, Xiaoping Song, and Zhimao Yang. "Copper-templated synthesis of gold microcages for sensitive surface-enhanced Raman scattering activity." RSC Adv. 4, no. 51 (2014): 27074–77. http://dx.doi.org/10.1039/c4ra03027c.

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Nanoparticle-aggregated Au microcages have been successfully synthesized from sacrificial hollow Cu microstructures, and exhibit remarkable surface-enhanced Raman scattering activity for 4-mercaptobenzoic acid.

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27

Minamiki, Tsukuru, and Ryoji Kurita. "Potentiometric detection of biogenic amines utilizing affinity on a 4-mercaptobenzoic acid monolayer." Analytical Methods 11, no. 9 (2019): 1155–58. http://dx.doi.org/10.1039/c8ay02616e.

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28

Yang, Qian-Qian, Wei Xiao, Wei Du, Qin Ouyang, and Ying-Chun Chen. "Asymmetric [4+2] annulations to construct norcamphor scaffolds with 2-cyclopentenone via double amine–thiol catalysis." Chemical Communications 54, no. 9 (2018): 1129–32. http://dx.doi.org/10.1039/c7cc09221k.

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29

Chen, Huaxiang, Tingting You, Li Jiang, Yukun Gao, and Penggang Yin. "Creating dynamic SERS hotspots on the surface of pH-responsive microgels for direct detection of crystal violet in solution." RSC Advances 7, no. 52 (2017): 32743–48. http://dx.doi.org/10.1039/c7ra05567f.

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30

Zhang, Chenmeng, Xiu Liang, Tingting You, Nan Yang, Yukun Gao, and Penggang Yin. "An ultrasensitive “turn-off” SERS sensor for quantitatively detecting heparin based on 4-mercaptobenzoic acid functionalized gold nanoparticles." Analytical Methods 9, no. 17 (2017): 2517–22. http://dx.doi.org/10.1039/c7ay00494j.

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We develop an ultrasensitive “turn off” Surface Enhanced Raman Spectroscopy (SERS) sensor for the detection of heparin based on the anti-aggregation of 4-mercaptobenzoic acid stabilized gold nanoparticles.

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31

Maya Girón, Julie V., Raquel V. Vico, Bruno Maggio, et al. "Role of the capping agent in the interaction of hydrophilic Ag nanoparticles with DMPC as a model biomembrane." Environmental Science: Nano 3, no. 2 (2016): 462–72. http://dx.doi.org/10.1039/c6en00016a.

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Citrate and 4-mercaptobenzoic acid capped AgNPs differentially interact with the DMPC model biomembrane. An explanation based on the surface charge density and on the chemical nature of the capping agent is discussed.

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32

Gühlke, Marina, Zsuzsanna Heiner, and Janina Kneipp. "Combined near-infrared excited SEHRS and SERS spectra of pH sensors using silver nanostructures." Physical Chemistry Chemical Physics 17, no. 39 (2015): 26093–100. http://dx.doi.org/10.1039/c5cp03844h.

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Combined surface-enhanced Raman scattering (SERS) and surface-enhanced hyper-Raman scattering (SEHRS) of a pH sensor, consisting of silver nanostructures and para-mercaptobenzoic acid and operating with near-IR excitation, is studied.

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33

Mukhtar, Asma, Arif Hussain, Faiza Younas, Sammer Yousuf, and Muhammad Saeed. "Facile synthesis of substituted 2-aroylbenzo[b]thiophen-3-ols to form novel triazole hybrids using click chemistry." RSC Advances 14, no. 15 (2024): 10270–79. http://dx.doi.org/10.1039/d4ra01146e.

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In the presence of triethylamine, 2-mercaptobenzoic acid (6) reacts with aryl bromomethyl ketones (8) to produce benzothiophenes (5), which can be subjected to a click reaction to construct benzothiophene-triazole hybrids (14).

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34

Sun, Qianqian, Shasha Zhang, Weini Huang, et al. "4-Mercaptobenzoic acid as a MALDI matrix for highly sensitive analysis of metals." Analyst 146, no. 5 (2021): 1543–47. http://dx.doi.org/10.1039/d1an00022e.

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4-Mercaptobenzoic acid was first introduced as a MALDI matrix for metal analysis. The developed method was successfully applied to the rapid screening and sensitive determination of metals in PM<sub>2.5</sub> samples.

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35

Lai, Wei, Jun Zhou, Yanting Liu, et al. "4MBA-labeled Ag-nanorod aggregates coated with SiO2: synthesis, SERS activity, and biosensing applications." Analytical Methods 7, no. 20 (2015): 8832–38. http://dx.doi.org/10.1039/c5ay01886b.

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A new nanostructure, silica-coated Ag nanorods (NRs) aggregate with 4-mercaptobenzoic acid molecules (4MBA-Ag NRs@SiO<sub>2</sub>), was prepared by a seed-mediated growth method and a modified Stöber method.

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36

Zhang, Jie, Mengzhong Cui, Shengyu Feng, Xiaomin Sun та Dacheng Feng. "Catalytic and Thermal 1,2-Rearrangement of (α-Mercaptobenzyl)trimethylsilane". Journal of Physical Chemistry A 113, № 41 (2009): 11007–14. http://dx.doi.org/10.1021/jp903646m.

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37

Aliyah, Mochammad Arfin Fardiansyah Nasution, Yulia Mariana Tesa Ayudia Putri, Jarnuzi Gunlazuardi, and Tribidasari Anggraningrum Ivandini. "Modification of carbon foam with 4-mercaptobenzoic acid functionalised gold nanoparticles for an application in a yeast-based microbial fuel cell." RSC Advances 12, no. 44 (2022): 28647–57. http://dx.doi.org/10.1039/d2ra05100a.

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Functionalisation of gold nanoparticles-modified carbon foam with 4-mercaptobenzoic acid was performed to improve its affinity toward microorganisms. The prepared electrode was evaluated for a microbial fuel cell with Candida fukuyamaensis yeast as the microorganisms.

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38

Kitahama, Yasutaka, Hiroaki Hayashi, Tamitake Itoh, and Yukihiro Ozaki. "Measurement of pH-dependent surface-enhanced hyper-Raman scattering at desired positions on yeast cells via optical trapping." Analyst 142, no. 20 (2017): 3967–74. http://dx.doi.org/10.1039/c7an00265c.

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At desired positions on yeast, pH-dependent surface-enhanced hyper-Raman scattering (SEHRS) spectra were recorded by focusing a near-infrared laser beam while silver nanoparticles (AgNPs) with 4-mercaptobenzoic acid (p-MBA) were simultaneously optically trapped.

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39

González, Miriam C. Rodríguez, Alejandro González Orive, Pilar Carro, Roberto C. Salvarezza, and Alberto Hernández Creus. "Structure and Electronic and Charge-Transfer Properties of Mercaptobenzoic Acid and Mercaptobenzoic Acid–Undecanethiol Mixed Monolayers on Au(111)." Journal of Physical Chemistry C 118, no. 51 (2014): 30013–22. http://dx.doi.org/10.1021/jp510398m.

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40

Imran, Muhammad, Farah Kanwal, Shoomaila Latif, Zafar Iqbal, and Liviu Mitu. "Heteronuclear Metal-organic Frameworks; Adsorption and Luminescence Aspects." Revista de Chimie 71, no. 4 (2020): 38–46. http://dx.doi.org/10.37358/rc.20.4.8041.

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Synthesis of heteronuclear metal organic frameworks (1 & 2) using 4-mercaptobenzoic acid (H2MBA) and 2,6-naphthalenedicarboxylic acid (2,6-NDA) was carried out followed by successful characterization with FTIR, SEM, EDX, 1H-NMR, TGA and PXD. Brunauer-Emmett-Teller (BET) and luminescence studies of these MOFs were also investigated.

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41

Hikawa, Hidemasa, та Isao Azumaya. "Mercaptobenzoic acid-palladium(0) complexes as active catalysts for S-benzylation with benzylic alcohols via (η3-benzyl)palladium(ii) cations in water". Org. Biomol. Chem. 12, № 31 (2014): 5964–72. http://dx.doi.org/10.1039/c4ob00688g.

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Mercaptobenzoic acid-palladium(0) complexes show high catalytic activity for S-benzylation with benzylic alcohols via the (η<sup>3</sup>-benzyl)palladium(ii) cation in water. The catalytic system can be performed using only 2.5 mol% Pd<sub>2</sub>(dba)<sub>3</sub> without the phosphine ligand or other additives.

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42

Pham, Xuan-Hung, Eunil Hahm, Kim-Hung Huynh, et al. "4-Mercaptobenzoic Acid Labeled Gold-Silver-Alloy-Embedded Silica Nanoparticles as an Internal Standard Containing Nanostructures for Sensitive Quantitative Thiram Detection." International Journal of Molecular Sciences 20, no. 19 (2019): 4841. http://dx.doi.org/10.3390/ijms20194841.

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In this study, SiO2@Au@4-MBA@Ag (4-mercaptobenzoic acid labeled gold-silver-alloy-embedded silica nanoparticles) nanomaterials were investigated for the detection of thiram, a pesticide. First, the presence of Au@4-MBA@Ag alloys on the surface of SiO2 was confirmed by the broad bands of ultraviolet-visible spectra in the range of 320–800 nm. The effect of the 4-MBA (4-mercaptobenzoic acid) concentration on the Ag shell deposition and its intrinsic SERS (surface-enhanced Raman scattering) signal was also studied. Ag shells were well coated on SiO2@Au@4-MBA in the range of 1–1000 µM. The SERS in

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43

Lang, Robert C., Craig M. Williams, and Mary J. Garson. "AN IMPROVED PREPARATION OF 4-AMINO-3-MERCAPTOBENZOIC ACID." Organic Preparations and Procedures International 35, no. 5 (2003): 520–24. http://dx.doi.org/10.1080/00304940309355864.

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44

Handa, Saori, Yingying Yu, and Masayuki Futamata. "Adsorbed state of p-mercaptobenzoic acid on silver nanoparticles." Vibrational Spectroscopy 72 (May 2014): 128–33. http://dx.doi.org/10.1016/j.vibspec.2014.03.007.

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45

KRISHNA, C. JOSHI, JAIN RENUKA, and NISHITH SAROJ. "Reactions of 3-Arylimino-2H-indol-2-ones with o-Mercaptobenzoic Acid and Salicylic Acid : Synthesis of Novel Spiro[2H-1,3-benzothiazine-2,3'-[3H]indole]-2,4( 1' H,3H)-diones." Journal of Indian Chemical Society Vol. 68, Nov 1991 (1991): 625–27. https://doi.org/10.5281/zenodo.6154499.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004 <em>Manuscript received 6 March 1991, accepted 7 November 1991</em> Reactions of 3-Arylimino-2<em>H</em>-indol-2-ones with o-Mercaptobenzoic Acid and Salicylic Acid : Synthesis of Novel Spiro[2<em>H</em>-1,3-benzothiazine-2,3'-[3<em>H</em>]indole]-2,4( 1' H, 3<em>H</em>)-diones.

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46

Prakash, Om, and Siva Umapathy. "Raman spectroscopy study of CdS nanorods and strain induced by the adsorption of 4-mercaptobenzoic acid." Journal of Chemical Physics 158, no. 13 (2023): 134719. http://dx.doi.org/10.1063/5.0142702.

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In this study, near- and off-resonance Raman spectra of cadmium sulfide (CdS) quantum rods (NRs) and 4-mercaptobenzoic acid (4-MBA) adsorbed CdS NRs are reported. The envelopes of characteristic optical phonon modes in the near-resonance Raman spectrum of CdS NRs are deconvoluted by following the phonon confinement model. As compared with off-resonant Raman spectra, optical phonon modes scattering cross section is amplified significantly in near-resonance Raman spectra through the Fröhlich interaction. The Huang–Rhys factor defining the strength of the Fröhlich interaction is estimated (∼0.468

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47

Tvedte, Laura M., and Christopher J. Ackerson. "Size-Focusing Synthesis of Gold Nanoclusters with p-Mercaptobenzoic Acid." Journal of Physical Chemistry A 118, no. 37 (2014): 8124–28. http://dx.doi.org/10.1021/jp5001946.

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48

Duarte, Anaí, Wilson Cunico, Claudio M. P. Pereira, Alex F. C. Flores, Rogério A. Freitag, and Geonir M. Siqueira. "Ultrasound promoted synthesis of thioesters from 2-mercaptobenzoxa(thia)zoles." Ultrasonics Sonochemistry 17, no. 2 (2010): 281–83. http://dx.doi.org/10.1016/j.ultsonch.2009.08.004.

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49

Wang, Huihui, Hitoshi Ohnuki, Hideaki Endo, and Mitsuru Izumi. "Preparation of Amperometric Glucose Biosensor Based on 4-Mercaptobenzoic Acid." Physics Procedia 14 (2011): 2–6. http://dx.doi.org/10.1016/j.phpro.2011.05.003.

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50

Trösch, Alexander, and Heinrich Vahrenkamp. "Zinkkomplexe des N,N,S-Liganden 2-Mercaptobenzyl-bis-(2-pyridylmethyl)amin." Zeitschrift für anorganische und allgemeine Chemie 627, no. 11 (2001): 2523. http://dx.doi.org/10.1002/1521-3749(200111)627:11<2523::aid-zaac2523>3.0.co;2-5.

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