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Journal articles on the topic 'Amido-group'

Author: Grafiati

Published: 5 June 2025

Last updated: 15 July 2025

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1

Pauls, Jochen, Soheila Chitsaz, and Bernhard Neumüller. "Alkoxo and Amido Compounds of Group 13." Phosphorus, Sulfur, and Silicon and the Related Elements 168, no. 1 (2001): 233–38. http://dx.doi.org/10.1080/10426500108546559.

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2

Havlík, Aleš, Martin Lamač, Jiří Pinkas, Aleš Růžička, and Michal Horáček. "Mixed amido-cyclopentadienyl group 4 metal complexes." RSC Advances 5, no. 73 (2015): 59154–66. http://dx.doi.org/10.1039/c5ra07742g.

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3

Liu, Jie Sheng, Shi Qiang Huang, and Shao Peng Wu. "Preparation of Amido Modified Silicone in Microemulsion." Key Engineering Materials 385-387 (July 2008): 497–500. http://dx.doi.org/10.4028/www.scientific.net/kem.385-387.497.

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A translucent amido modified microemulsion was synthesized by the adding of amido silane coupling agent. Transmission electron microscope (TEM), Fourier Transform Infrared Spectra (FT-IR), Photon Correlation Spectroscopy (PCS) were used to characterize the structures and properties of amido microemulsion, respectively. IR spectroscopy confirmed that amido group was successfully introduced into the polysiloxane microemulsion. TEM images indicated that the granules agglomerated heavily when the coupling agent was in a larger content. The effects of PH values, amount of coupling agent on the size and the configuration of the amido microemulsion were investigated. The results indicated that the properties of amido microemulsion were stable when the microemulsion was under weak acid condition (pH=3-7). When the amount of coupling agent increased, the particles size of microemulsion increased and the particle size distribution became narrow.

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4

Dange, Deepak, Amelia Davey, Joseph A. B. Abdalla, Simon Aldridge, and Cameron Jones. "Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene." Chemical Communications 51, no. 33 (2015): 7128–31. http://dx.doi.org/10.1039/c5cc01772f.

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The first examples of an amido-distibene and a boryl dibismuthene (see picture) have been prepared by reaction of a lithium boryl complex with extremely bulky amido-group 15 dihalide precursor compounds.

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5

McKnight, Andrew L., and Robert M. Waymouth. "Group 4ansa-Cyclopentadienyl-Amido Catalysts for Olefin Polymerization." Chemical Reviews 98, no. 7 (1998): 2587–98. http://dx.doi.org/10.1021/cr940442r.

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6

Foster, Patrick, James C. W. Chien, and Marvin D. Rausch. "New ethylene bridged monofluorenyl-amido group 4 complexes." Journal of Organometallic Chemistry 545-546 (January 1997): 35–38. http://dx.doi.org/10.1016/s0022-328x(97)00226-x.

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7

FORT, M., and L. L. LLOYD. "The Development of the Amido Group in Wool." Journal of the Society of Dyers and Colourists 30, no. 3 (2008): 73–78. http://dx.doi.org/10.1111/j.1478-4408.1914.tb00795.x.

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8

Qin, Wenling, Xiaoyan Wu, Lu Xue, Shilong Luo, Shiqi Jia та Jun Ao. "K2S2O8-Activated Friedel–Crafts Type Alkylation of Indoles with α-Amido Sulfones". Synthesis 49, № 22 (2017): 5017–24. http://dx.doi.org/10.1055/s-0036-1589073.

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A K2S2O8-activated regioselective alkylation of α-amido sulfones at the C-3 position of indoles is reported. The protocol developed herein provides an alternative new strategy to the previous approach by using Lewis acid, clay, and resin as catalyst for this Friedel–Crafts type alkylation of indoles with α-amido sulfones. The formed product bears a versatile transformable sulfone group and an amino group. The reaction condition is tolerant to a wide range of substrates, including a series of indoles with electron-withdrawing and electron-donating groups at different positions. Moreover, a variety of α-substituted phenylamido sulfones and some α-aliphatic amido sulfones also give the desired products in modest yield. Furthermore, a preliminary mechanism study was performed and the plausible reaction mechanism is discussed.

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9

Pham, John W., Ishwar Radhakrishnan, and Erik J. Sontheimer. "Thermodynamic and structural characterization of 2′-nitrogen-modified RNA duplexes." Nucleic Acids Research 32, no. 11 (2004): 3446–55. http://dx.doi.org/10.1093/nar/gkh658.

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Abstract 2′-aminonucleosides are commonly used as sites of post-synthetic chemical modification within nucleic acids. As part of a larger cross-linking strategy, we appended alkyl groups onto the N2′ position of 2′-amino-modified RNAs via 2′-ureido and 2′-amido linkages. We have characterized the thermodynamics of 2′-amino, 2′-alkylamido and 2′-alkylureido-modified RNA duplexes and show that 2′-ureido-modified RNAs are significantly more stable than analogous 2′-amido-modified RNAs. Using NMR spectroscopy and NMR-based molecular modeling of 2′-modified RNA duplexes, we examined the effects that 2′-nitrogen modifications have on RNA helices. Our data suggest that the 2′-ureido group forms a specific intra-nucleoside interaction that cannot occur within 2′-amido-modified helices. These results indicate that 2′-ureido modifications are superior to analogous 2′-amido ones for applications that require stable base pairing.

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10

Pauls, Jochen, Soheila Chitsaz, and Bernhard Neumuller. "ChemInform Abstract: Alkoxo and Amido Compounds of Group 13." ChemInform 33, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.200203256.

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11

Sun, Chen, Victoria F. Oswald, Ethan A. Hill, Joseph W. Ziller, and A. S. Borovik. "Investigation of iron–ammine and amido complexes within a C3-symmetrical phosphinic amido tripodal ligand." Dalton Transactions 50, no. 32 (2021): 11197–205. http://dx.doi.org/10.1039/d1dt01032h.

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12

Stankevič, Marek. "Diastereoselective desymmetrization of diarylphosphinous acid-borane amides under Birch reduction." Organic & Biomolecular Chemistry 13, no. 21 (2015): 6082–102. http://dx.doi.org/10.1039/c4ob02440k.

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13

Devillard, M., C. Alvarez Lamsfus, V. Vreeken, L. Maron, and J. I. van der Vlugt. "Versatile coordination of a reactive P,N-ligand toward boron, aluminum and gallium and interconversion reactivity." Dalton Transactions 45, no. 27 (2016): 10989–98. http://dx.doi.org/10.1039/c6dt02087a.

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14

Mu, Ying, Warren E. Piers, Mary-Anne MacDonald та Michael J. Zaworotko. "Attachment of C5Me4HSi(Me2)NH-t-C4H9 to yttrium via amine elimination. X-ray structure of [(η5-C5Me4)Si(Me2)-η1-N-t-C4H9]YN(SiMe3)2". Canadian Journal of Chemistry 73, № 12 (1995): 2233–38. http://dx.doi.org/10.1139/v95-277.

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Reaction of the homoleptic yttrium amido complex Y[N(SiMe3)2]3 with C5Me4HSiMe2N(H)-t-C4H9, Cp*HSiNHR, at 100 °C resulted in elimination of 2 equivalents of HN(SiMe3)2 and attachment of the Cp-amido donor to yttrium. The product (Cp*SiNR)YN(SiMe3)2, 1, was isolated in 40% yield and was characterized crystallographically (triclinic, space group [Formula: see text] a = 8.9759(23) Å, b = 9.504(7) Å, c = 18.294(6) Å, V = 1423.4(12) Å3, Z = 2, R = 0.061, Rw = 0.053). Metrical parameters associated with the N(SiMe3)2 ligand were suggestive of weak β-SiC agostic interactions that stabilize the electron-deficient yttrium center. Alkylation of 1 resulted in unstable alkyl derivatives that could not be isolated. Keywords: cyclopentadienyl-amido, amine elimination, yttrium complex.

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15

Lin, Hai Yan, Yong Fu Yang, and Yu Jiang Wang. "Study on Grinding Aids of Different Organic Group." Advanced Materials Research 476-478 (February 2012): 1702–8. http://dx.doi.org/10.4028/www.scientific.net/amr.476-478.1702.

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Organic substances containing hydroxyl group and alcohol amine group were chosen in this paper and the effects of different organic group on powder properties and physical performance of cement pastes were studied using various methods of analysis, such as particle size analysis, fluidness analysis and XRD. The results show that monohydric alcohols have a neglectable aid-grinding effect. For Polyhydric alcohols and ethanol amine, the absorption capacity of the hydroxyl group or amido on the surface of the powder may increase in relation to the increase in groups, which can increase fineness but cannot improve the fluidity. For Diethanolamine and Triethanolamine, the absorption on the powder mainly depends on the hydroxyl group, but the amido has a strong electrostatic repulsive force, so the dispersion of the powder not only comes from high steric hindrance effect, but also the electrostatic repulsive force, which can improve the powder’s dispersity, reduce sieve residue and increase the fluidity. This research paper provides a theoretical guide for the application of grinding aids.

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16

Kunishima, Munetaka, Daiki Kato, Nobu Kimura, Masanori Kitamura, Kohei Yamada, and Kazuhito Hioki. "Potent triazine-based dehydrocondensing reagents substituted by an amido group." Beilstein Journal of Organic Chemistry 12 (August 24, 2016): 1897–903. http://dx.doi.org/10.3762/bjoc.12.179.

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This study describes the synthesis of triazine-based dehydrocondensing reagents substituted by amido substituents and demonstrates their efficiency for dehydrocondensing reactions in MeOH and THF. N-Phenylbenzamido-substituted chlorotriazine is readily converted to a stable, non-hygroscopic triazinylammonium-based dehydrocondensing reagent that is superior to 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) in terms of its reactivity in dehydrocondensing reactions.

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17

McKnight, Andrew L., Md Athar Masood, Robert M. Waymouth, and Daniel A. Straus. "Selectivity in Propylene Polymerization with Group 4 Cp−Amido Catalysts." Organometallics 16, no. 13 (1997): 2879–85. http://dx.doi.org/10.1021/om9609628.

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18

Singh, Anupam, U. Anandhi, Maria Agostina Cinellu, and Paul R. Sharp. "Diimine supported group 10 hydroxo, oxo, amido, and imido complexes." Dalton Transactions, no. 17 (2008): 2314. http://dx.doi.org/10.1039/b715663d.

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19

Schmidtke, Hans-Herbert, Thomas Schönherr, Wilhelm Kuchen, and Manfred Fuchs. "The ligand field potential of the amido group in transition group ion phosphinothioicamido chelates." Chemical Physics Letters 124, no. 2 (1986): 159–63. http://dx.doi.org/10.1016/0009-2614(86)85136-3.

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20

Xu, Jiaxi, Kun Yang, Zhenjiang Li, et al. "Tunable intramolecular H-bonding promotes benzoic acid activity in polymerization: inspiration from nature." Polym. Chem. 8, no. 41 (2017): 6398–406. http://dx.doi.org/10.1039/c7py01451a.

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Intramolecular H-bonding of ortho-amido group(s) tuned benzoic acid into strong Brønsted acid active in ring-opening polymerizations of lactones and trimethylene carbonate at room temperature in solutions.

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21

Bomparola, Roberta, Robert P. Davies, Stefan Hornaeur, and Andrew J. P. White. "Lithium heterocuprates: the influence of the amido group on organoamidocuprate structures." Dalton Trans. 43, no. 38 (2014): 14359–67. http://dx.doi.org/10.1039/c4dt00965g.

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The structural isomers of a number of lithium heteroamidocuprates LiCuR(NR′2) have been studied in the solid state and in solution, with the steric and electronic properties of the amido group (NR′2) shown to significantly influence the solid-state structures and the position of the solution equilibrium.

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22

Decken, Andreas, Robert A. Gossage, and Paras N. Yadav. "Oxazoline chemistry. Part VIII. Synthesis and characterization of a new class of pincer ligands derived from the 2-(o-anilinyl)-2-oxazoline skeleton Applications to the synthesis of group X transition metal catalysts." Canadian Journal of Chemistry 83, no. 8 (2005): 1185–89. http://dx.doi.org/10.1139/v05-163.

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The synthesis and characterization of a new and readily synthesized class of potentially anionic pincer ligands with C1 point group symmetries is described. These materials can be made via amide coupling of a 2-(2′-anilinyl)-2-oxazoline unit with picolinic acid; the incorporation of enantiopure oxazoline fragments facilitates the construction of chiral C1 pincers. Treatment of the free ligands with Pd metal sources leads to the formation of amidoPd pincer complexes in good yield. One of these Pd complexes has been characterized by single crystal X-ray diffraction methods, which confirms the proposed tridentate binding mode of the ligand and the formation of an amido NPd bond. The metal complexes have been shown to be suitable precusors for catalytically active Pd species that are useful for CC bond forming reactions, notably the Heck reaction under standard conditions. Key words: oxazoline, 4,5-dihydro-2-oxazole, palladium, pincer ligand, amido, Heck reaction.

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23

Sun, Yanjie, Shuhui Li, Takeshi Shiono, and Zhengguo Cai. "Substituent Effects of Adamantyl Group on Amido Ligand in Syndiospecific Polymerization of Propylene with Ansa-Dimethylsilylene(Fluorenyl)(Amido) Zirconium Complex." Polymers 9, no. 11 (2017): 632. http://dx.doi.org/10.3390/polym9110632.

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24

Cundari, Thomas R., and Mark S. Gordon. "Small molecule elimination from Group IVB (titanium, zirconium, hafnium) amido complexes." Journal of the American Chemical Society 115, no. 10 (1993): 4210–17. http://dx.doi.org/10.1021/ja00063a044.

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25

McKnight, Andrew L., and Robert M. Waymouth. "ChemInform Abstract: Group 4 ansa-Cyclopentadienyl-Amido Catalysts for Olefin Polymerization." ChemInform 30, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199904274.

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26

Qin, Duwei, Fubin Han, Yingming Yao, Yong Zhang, and Qi Shen. "Migration of amide to imine group of lanthanide Schiff base complexes: effect of amido group." Dalton Transactions, no. 28 (2009): 5535. http://dx.doi.org/10.1039/b904580e.

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27

Padwa, Albert, William S. Kissell, and Cheryl K. Eidell. "Cyclizationcycloaddition cascades for the construction of azapolycyclic ring systems." Canadian Journal of Chemistry 79, no. 11 (2001): 1681–93. http://dx.doi.org/10.1139/v01-154.

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Cyclic 2-amidofuranones were obtained from the Rh(II)-catalyzed reaction of alpha-diazoketo substituted pyrrolidine derivatives. These compounds are derived by a [1,4]-hydrogen transfer from an initially formed carbonyl ylide dipole. Acylation of the amido-substituted furanone with pivalyl chloride provided a fused amidofuran, which underwent bimolecular Diels-Alder cycloaddition with N-phenylmaleimide. The Rh(II)-catalyzed decomposition of ethyl 2-diazo-3-oxo-(2-oxo-1-pent-4-enoyl-pyrrolidine-3-yl)propionate was also examined. In this case, the alkenyl group tethered to the amido carbonyl underwent smooth intramolecular [4+2]-cycloaddition with the amidofuran obtained from the acylation reaction. An alternate route for the synthesis of cyclic amidofurans was developed using a Pummerer induced cyclization of the thiophenyl substituted acetal derived from the aldol reaction of methoxyphenylsulfanyl acetaldehyde with α-valerolactam. Treatment of the amido-substituted acetal with dimethyl(methylthio)sulfonium tetrafluoroborate (DMTSF) generated an oxonium ion, which readily cyclized onto the adjacent carbonyl group. The amidofuran that was formed underwent an intramolecular Diels-Alder reaction when heated at 110°C in toluene. Subsequent ring opening of the transient [4+2]-cycloadduct followed by elimination of methanol and tautomerization of the resulting cyclohexadienone gave rise to the observed phenolic lactam in good overall yield.Key words: intramolecular, cyclization, Diels-Alder, diazo-ketoamide, rhodium(II).

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28

Tao, Siying, Menglin Fan, Hockin H. K. Xu, et al. "The remineralization effectiveness of PAMAM dendrimer with different terminal groups on demineralized dentin in vitro." RSC Advances 7, no. 87 (2017): 54947–55. http://dx.doi.org/10.1039/c7ra11844a.

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The aim of this study was to examine the dentin remineralization extent that poly(amido amine) (PAMAM) induces quantitatively, and select the most effective kind of PAMAM with a certain terminal group for dentin remineralization, both for the first time.

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29

Monleón, Alicia, Gonzalo Blay та José R. Pedro. "Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones". Molecules 27, № 12 (2022): 3763. http://dx.doi.org/10.3390/molecules27123763.

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A convenient procedure of synthesis of N-carbamoyl-protected propargylic amines substituted with a cyclopropyl group from α-amido sulfones and cyclopropylacetylene is described. The reaction is catalyzed by a chiral BINOL-type zinc complex and provides the corresponding products in good yields and enantioselectivities.

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30

Nandi, Mandira, Saikat Santra, Bidyut Akhuli, and Pradyut Ghosh. "Threading of various ‘U’ shaped bidentate axles into a heteroditopic macrocyclic wheel via NiII/CuII templation." Dalton Transactions 46, no. 23 (2017): 7421–33. http://dx.doi.org/10.1039/c7dt00699c.

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The Ni<sup>II</sup>/Cu<sup>II</sup> templated threading of various terminal group embedded ‘U’ shaped axles into an amido–amine macrocyclic wheel towards the development of a new generation of [2]pseudorotaxanes via [3 + 2] coordination assisted by other non-covalent interactions.

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31

Abo-Amer, Anwar, Mahmoud Al-Refai, Richard J. Puddephatt, and Basem F. Ali. "3-Bromo-N-(3,5-di-tert-butylphenyl)propanamide." Acta Crystallographica Section E Structure Reports Online 70, no. 7 (2014): o770. http://dx.doi.org/10.1107/s1600536814012094.

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The title compound, C17H26BrNO, exhibits a small twist between the amide residue and the benzene ring [C—N—C—C torsion angle = 29.4 (5)°]. In the crystal, the amido NH group is involved in N—H...O hydrogen bonding, which connects molecules into chains parallel to thecaxis.

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32

Gade, Lutz H. "Tripodal Amido Complexes: Molecular “Claws” in Main Group and Transition Metal Chemistry." Accounts of Chemical Research 35, no. 7 (2002): 575–82. http://dx.doi.org/10.1021/ar010116f.

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33

Rasika Dias, H. V., Ziyun Wang, and Simon G. Bott. "Preparation of group 4 metal complexes of a bulky amido-fluorenyl ligand." Journal of Organometallic Chemistry 508, no. 1-2 (1996): 91–99. http://dx.doi.org/10.1016/0022-328x(95)05803-w.

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34

Li, Huo, Jun-Ran Li, and Fu-Hui Liao. "The comparison between carboxyl, amido and hydroxy group in influencing electrorheological performance." Korea-Australia Rheology Journal 23, no. 1 (2011): 17–23. http://dx.doi.org/10.1007/s13367-011-0003-9.

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35

Ohyanagi, Manshi, Hiroyuki Nishide, Koichi Suenaga, and Eishun Tsuchida. "Synthesis of Polyorganosiloxane withN-(4-Pyridyl)amido Group on the Side Chain." Chemistry Letters 16, no. 12 (1987): 2309–10. http://dx.doi.org/10.1246/cl.1987.2309.

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36

Hammal, Lamouri, Laurent El Kaïm, Samira Baaziz, Mansour Kerim, and Marie Cordier. "Metal-free Deamidative Ugi Access to Isoindolinones." Synlett 29, no. 14 (2018): 1842–46. http://dx.doi.org/10.1055/s-0037-1610189.

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A two-step isoindolone synthesis has been achieved by using an Ugi/oxidative vicarious nucleophilic substitution sequence starting from 3-nitrobenzoic acid and aromatic aldehydes. Loss of the amido group was observed as well as a further oxidative process towards hydroxyisoindolone derivatives after prolonged stirring open to the atmosphere.

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37

Raston, Colin L., Brian W. Skelton, Vicki-Anne Tolhurst, and Allan H. White. "Bis-amido- complexes of heavier Group 15 metal chlorides with the sterically hindered, N-functionalised amido ligand, [{2-(6-Me)C5H3N}NSiMe3]−." Polyhedron 17, no. 5-6 (1998): 935–42. http://dx.doi.org/10.1016/s0277-5387(97)00243-x.

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38

Tang, Shi, ShuHua Li, Dong Zhou, HuiQiong Zeng та NaiXing Wang. "Stereoselective C(sp3)-C(sp2) Negishi coupling of (2-amido-1-phenylpropyl)zinc compounds through the steric control of β-amido group". Science China Chemistry 56, № 9 (2013): 1293–300. http://dx.doi.org/10.1007/s11426-013-4880-2.

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39

Dhudmal, Chaya N., Dhanraj O. Biradar, Maddipatla V. Satyanarayana, and Basi V. Subba Reddy. "Stereoselective Total Synthesis of 1,4-Dideoxy-1,4-imino-L-ribitol by an Intramolecular Ring Opening of Epoxide with a Tethered Amide." Natural Product Communications 13, no. 8 (2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300821.

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Stereoselective total synthesis of 1,4-dideoxy-1,4-imino-L-ribitol has been accomplished from D-glucose. The key step involved in this synthesis is the regioselective ring-opening of the epoxide with a tethered amido group to give the N-tosyl-3,6-dideoxy-3,6-imino-1,2- O-isopropylidene-α-D-glucofuranose.

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40

Diop, Mouhamadou Birame, Libasse Diop, and Allen G. Oliver. "Crystal structure ofN-[(methylsulfanyl)carbonyl]urea." Acta Crystallographica Section E Crystallographic Communications 72, no. 3 (2016): 325–27. http://dx.doi.org/10.1107/s2056989016002322.

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The almost planar (r.m.s. deviation = 0.055 Å) title compound, (MeS)C(O)NHC(O)NH2, was formed during an attempted crystallization of dimethyl cyanocarbonimidodithioate with CrO2Cl2; an unexpected redox reaction converted the cyanocarbonimido moiety to a urea group and removed one methylthiol group. In the crystal, hydrogen-bonding interactions from the amide and amido N—H groups to carbonyl O atoms of neighbouring molecules result in [010] ribbon-like chains.

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41

Hadlington, Terrance J., Jiaye Li, and Cameron Jones. "Synthesis and characterization of extremely bulky amido-germanium(II) halide complexes." Canadian Journal of Chemistry 92, no. 6 (2014): 427–33. http://dx.doi.org/10.1139/cjc-2013-0394.

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The extremely bulky aryl/silyl secondary amines, HN(Ar)(SiMe3), Ar = C6H2-i-Pr2(CPh3)-2,6,4 (LDipH), C6H2{C(H)Ph2}2-i-Pr-2,6,4 (L†H), or C6H2{C(H)Ph2}2-t-Bu-2,6,4 (Lt-BuH), have been synthesized via salt metathesis reactions between the appropriate lithium anilide complex and ClSiMe3. The related diaryl secondary amines, HN(Ar*)(R), Ar* = C6H2{C(H)Ph2}2Me-2,6,4 and R = C6H3Me2-3,5 (LMeH), C6H3(CF3)2-3,5 (LCF3H), or C6H2-i-Pr3-2,4,6 (LTripH), were prepared via palladium catalyzed cross-coupling reactions. Three of the amines were crystallographically characterized. Treatment of GeCl2·dioxane with 1 equiv. of each of the deprotonated amines led to the isolation of the amido-germanium(II) chloride complexes, [LGeCl] (L = L†, Lt-Bu, LCF3, or LTrip). Similarly, reaction of the known amido-digermyne, [L*Ge–GeL*] (L* = –N(Ar*)(SiMe3)), with I2 resulted in the oxidative cleavage of the Ge–Ge bond of the digermyne, and the formation of the first two-coordinate amido-germanium(II) iodide complex, [L*GeI]. Crystallographic characterization of [Lt-BuGeCl] and [L*GeI] revealed both to have similar monomeric structures. The compounds described in this study should prove useful as synthons for synthetic chemists working in the field of low oxidation state main group chemistry.

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42

Li, Jiaye, Andreas Stasch, Christian Schenk, and Cameron Jones. "Extremely bulky amido-group 14 element chloride complexes: Potential synthons for low oxidation state main group chemistry." Dalton Transactions 40, no. 40 (2011): 10448. http://dx.doi.org/10.1039/c1dt10678c.

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43

Burford, Richard J., Alyssa Yeo, and Michael D. Fryzuk. "Dinitrogen activation by group 4 and group 5 metal complexes supported by phosphine-amido containing ligand manifolds." Coordination Chemistry Reviews 334 (March 2017): 84–99. http://dx.doi.org/10.1016/j.ccr.2016.06.015.

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44

Hsieh, Chang-Chih, Hon Man Lee, and Yih-Chern Horng. "N-[2-(Methylsulfanyl)phenyl]-2-sulfanylbenzamide." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2400. http://dx.doi.org/10.1107/s1600536812029765.

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In the title compound, C14H13NOS2, the S atom with the methyl group is involved in an intramolecular hydrogen bond with the amido H atom. In the crystal, the sulfanyl H atoms form intermolecular hydrogen bonds with the O atoms, connecting the molecules into zigzag chains along thecaxis. The two aromatic rings exhibit a small interplanar angle of 16.03 (9)°.

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45

Destarac, Mathias, Juliette Ruchmann-Sternchuss, Eric Van Gramberen, Xavier Vila та Samir Z. Zard. "α-Amido Trifluoromethyl Xanthates: A New Class of RAFT/MADIX Agents". Molecules 29, № 10 (2024): 2174. http://dx.doi.org/10.3390/molecules29102174.

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Abstract:

Xanthates have long been described as poor RAFT/MADIX agents for styrene polymerization. Through the determination of chain transfer constants to xanthates, this work demonstrated beneficial capto-dative substituent effects for the leaving group of a new series of α-amido trifluoromethyl xanthates, with the best effect observed with trifluoroacetyl group. The previously observed Z-group activation with a O-trifluoroethyl group compared to the O-ethyl counterpart was quantitatively established with Cex = 2.7 (3–4 fold increase) using the SEC peak resolution method. This study further confirmed the advantageous incorporation of trifluoromethyl substituents to activate xanthates in radical chain transfer processes and contributed to identify the most reactive xanthate reported to date for RAFT/MADIX polymerization of styrene.

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Cai, Hu, Wai Han Lam, Xianghua Yu, et al. "Synthesis, Characterization, and Theoretical Studies of Group 4 Amido Hydrotris(pyrazolyl)borate Complexes." Inorganic Chemistry 42, no. 9 (2003): 3008–15. http://dx.doi.org/10.1021/ic026063v.

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47

Stahl, Lothar. "Bicyclic and tricyclic bis(amido)cyclodiphosph(III)azane compounds of main group elements." Coordination Chemistry Reviews 210, no. 1 (2000): 203–50. http://dx.doi.org/10.1016/s0010-8545(00)00312-x.

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48

Kim, Young Kwan, Tom Livinghouse, and John E. Bercaw. "Intramolecular alkene hydroaminations catalyzed by simple amido derivatives of the Group 3 metals." Tetrahedron Letters 42, no. 16 (2001): 2933–35. http://dx.doi.org/10.1016/s0040-4039(01)00346-x.

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49

Betley, Theodore A., Baixin A. Qian, and Jonas C. Peters. "Group VIII Coordination Chemistry of a Pincer-Type Bis(8-quinolinyl)amido Ligand." Inorganic Chemistry 47, no. 24 (2008): 11570–82. http://dx.doi.org/10.1021/ic801047s.

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Rajesh, A., and S. Sivaram. "Polymerization of ethylene using amido functional half-sandwich complexes of group 4 metals." Polymer Engineering & Science 51, no. 10 (2011): 2103–8. http://dx.doi.org/10.1002/pen.22132.

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