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Journal articles on the topic 'Non-innocent'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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1

Berben, Louise A., Bas de Bruin, and Alan F. Heyduk. "Non-innocent ligands." Chemical Communications 51, no. 9 (2015): 1553–54. http://dx.doi.org/10.1039/c4cc90480j.

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2

Fileva, Iskra. "Envy's Non-Innocent Victims." Journal of Philosophy of Emotion 1, no. 1 (2019): 1–22. http://dx.doi.org/10.33497/jpe.v1i1.25.

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3

Murphy, Michelle. "Toward Non-innocent Reassemblies." Engaging Science, Technology, and Society 2 (August 1, 2016): 128. http://dx.doi.org/10.17351/ests2016.94.

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4

Butin, Kim P., Elena K. Beloglazkina, and Nikolai V. Zyk. "Metal complexes with non-innocent ligands." Russian Chemical Reviews 74, no. 6 (2005): 531–53. http://dx.doi.org/10.1070/rc2005v074n06abeh000977.

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5

Alves, Hélder Vinagreiro, Mariana Mello Breyner, Sílvia Fontinha Nunes, Bruno Diogo Pereira, Luís Filipe Silva, and Joana Soares. "Are victims also judged more positively if they say their lives are just?" PSICOLOGIA 29, no. 2 (2015): 71–80. http://dx.doi.org/10.17575/rpsicol.v29i2.1064.

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Non-victims who express high versus low personal belief in a just world (PBJW) are judged as having more social value, both social utility (i.e., market value) and social desirability (i.e., affective value). Our goal was to test whether this pattern differed when the targets were presented as innocent or non-innocent victims of enduring suffering. A hundred and eighty-six participants of both sexes took part in our 2 (degree of PBJW expressed: high/low) X 3 (Target identity: innocent victim/ non-innocent victim/ non-victim) between-subjects experimental study. Participants rated the targets o

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6

Vlcek, Antonin. "Dithiolenes and non-innocent redox-active ligands." Coordination Chemistry Reviews 254, no. 13-14 (2010): 1357. http://dx.doi.org/10.1016/j.ccr.2010.01.015.

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7

Dutta, Debarpan, Suvendu Maity, Suman Kundu, and Prasanta Ghosh. "Mixed-valence di-ruthenium(ii,iii) complexes of redox non-innocent N-aryl-o-phenylenediamine derivatives." Dalton Transactions 50, no. 22 (2021): 7791–803. http://dx.doi.org/10.1039/d1dt00779c.

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8

Johnson, Nicolas A., Samuel R. Wolfe, Humayun Kabir, et al. "Deconvoluting the Innocent vs. Non-Innocent Behavior of N ,N -Diethylphenylazothioformamide Ligands with Copper Sources." European Journal of Inorganic Chemistry 2017, no. 47 (2017): 5576–81. http://dx.doi.org/10.1002/ejic.201701097.

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9

Singha, Asmita, Kaustuv Mittra, and Abhishek Dey. "Effect of hydrogen bonding on innocent and non-innocent axial ligands bound to iron porphyrins." Dalton Transactions 48, no. 21 (2019): 7179–86. http://dx.doi.org/10.1039/c8dt03852j.

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10

Polukeev, Alexey V., and Ola F. Wendt. "Iridium complexes with aliphatic, non-innocent pincer ligands." Journal of Organometallic Chemistry 867 (July 2018): 33–50. http://dx.doi.org/10.1016/j.jorganchem.2017.12.009.

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11

Blanchard, Sébastien, Etienne Derat, Marine Desage-El Murr, Louis Fensterbank, Max Malacria, and Virginie Mouriès-Mansuy. "Non-Innocent Ligands: New Opportunities in Iron Catalysis." European Journal of Inorganic Chemistry 2012, no. 3 (2011): 376–89. http://dx.doi.org/10.1002/ejic.201100985.

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12

Miranda, Katrina M. "Coordination of non-innocent nitrogen oxide ligands: terminology." JBIC Journal of Biological Inorganic Chemistry 24, no. 3 (2019): 315–16. http://dx.doi.org/10.1007/s00775-019-01659-0.

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13

Matelková, Kristína, Katrin Ossberger, Juraj Hudák, Jaroslav Vatrál, Roman Boča, and Wolfgang Linert. "Redox activity of some non-innocent amino acids." Monatshefte für Chemie - Chemical Monthly 144, no. 7 (2013): 937–49. http://dx.doi.org/10.1007/s00706-013-0972-0.

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14

Kaim, Wolfgang, and Brigitte Schwederski. "Non-innocent ligands in bioinorganic chemistry—An overview." Coordination Chemistry Reviews 254, no. 13-14 (2010): 1580–88. http://dx.doi.org/10.1016/j.ccr.2010.01.009.

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15

Mondal, Manas Kumar, Abul Kalam Biswas, Bishwajit Ganguly, and Chandan Mukherjee. "Unprecedented iminobenzosemiquinone and iminobenzoquinone coordinated mononuclear Cu(ii) complex formation under air." Dalton Transactions 44, no. 20 (2015): 9375–81. http://dx.doi.org/10.1039/c4dt03263b.

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Ligand H4LS(AP/AP) comprised of two orthogonally placed non-innocent unit that were bridged by a common -ortho S atom. It reacted with CuCl<sub>2</sub>·2H<sub>2</sub>O and provided a mononuclear diamagnetic Cu(ii) complex where two non-innocent units were in two different oxidation states.

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16

Periyasamy, Ganga, Neil A. Burton, Ian H. Hillier, et al. "The dithioleneligand—‘innocent’ or ‘non-innocent’? A theoretical and experimental study of some cobalt–dithiolene complexes." Faraday Discuss. 135 (2007): 469–88. http://dx.doi.org/10.1039/b607144a.

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17

Alves, Hlder, and Isabel Correia. "A first approach to perceptions of social norms regarding reactions towards innocent and non-innocent victims." Portugese Journal of Social Sciences 8, no. 2 (2009): 133–45. http://dx.doi.org/10.1386/pjss.8.2.133/1.

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18

Cappillino, Patrick J., Harry D. Pratt, Nicholas S. Hudak, Neil C. Tomson, Travis M. Anderson, and Mitchell R. Anstey. "Application of Redox Non-Innocent Ligands to Non-Aqueous Flow Battery Electrolytes." Advanced Energy Materials 4, no. 1 (2013): 1300566. http://dx.doi.org/10.1002/aenm.201300566.

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19

Gushchin, A., R. Llusar, D. Recatalá, and P. Abramov. "First heteroleptic Mo3S7 clusters containing non-innocent phenanthroline ligands." Russian Journal of Coordination Chemistry 38, no. 3 (2012): 173–77. http://dx.doi.org/10.1134/s1070328412030050.

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20

Berben, Louise A. "Catalysis by Aluminum(III) Complexes of Non-Innocent Ligands." Chemistry - A European Journal 21, no. 7 (2014): 2734–42. http://dx.doi.org/10.1002/chem.201405400.

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21

Weger, Michael, Raphael K. Grötsch, Maximilian G. Knaus, et al. "Non‐Innocent Methylene Linker in Bridged Lewis Pair Initiators." Angewandte Chemie International Edition 58, no. 29 (2019): 9797–801. http://dx.doi.org/10.1002/anie.201902833.

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22

Kaim, Wolfgang. "Chelate rings of different sizes with non-innocent ligands." Dalton Transactions 48, no. 24 (2019): 8521–29. http://dx.doi.org/10.1039/c9dt01411j.

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23

Gurdal, Yeliz, Sandra Luber, Jürg Hutter, and Marcella Iannuzzi. "Non-innocent adsorption of Co-pyrphyrin on rutile(110)." Physical Chemistry Chemical Physics 17, no. 35 (2015): 22846–54. http://dx.doi.org/10.1039/c5cp02767e.

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24

Buncic, Gojko, Zhiguang Xiao, Simon C. Drew, Jonathan M. White, Anthony G. Wedd, and Paul S. Donnelly. "Copper complexes of a novel non-innocent quadridentate ligand." Chemical Communications 48, no. 20 (2012): 2570. http://dx.doi.org/10.1039/c2cc16658e.

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25

Jović, Marija, Sebastian Torker, and Peter Chen. "Non-innocent Character of Oxyanions in Ruthenium Metathesis Catalysts." Organometallics 30, no. 15 (2011): 3971–80. http://dx.doi.org/10.1021/om200124z.

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26

Kaim, Wolfgang, Atanu Das, Jan Fiedler, Stanislav Záliš, and Biprajit Sarkar. "NO and NO2 as non-innocent ligands: A comparison." Coordination Chemistry Reviews 404 (February 2020): 213114. http://dx.doi.org/10.1016/j.ccr.2019.213114.

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27

Guntheroth, Warren G. "Innocent Murmurs: A Suspect Diagnosis in Non-Pregnant Adults." American Journal of Cardiology 104, no. 5 (2009): 735–37. http://dx.doi.org/10.1016/j.amjcard.2009.04.031.

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28

Harmer, Colin P., Chongin Pak, Joshua T. Greenfield, Adedoyin N. Adeyemi, Eranga H. Gamage, and Kirill Kovnir. "Non-innocent Intercalation of Diamines into Tetragonal FeS Superconductor." ACS Applied Energy Materials 4, no. 1 (2021): 42–46. http://dx.doi.org/10.1021/acsaem.0c02996.

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29

Ghorai, Samir, and Chandan Mukherjee. "Copper(II)-Mediated Transformation of a Tridentate Non-Innocent Ligand into a Tetradentate Salen-Type Innocent Ligand." Chemistry - An Asian Journal 9, no. 12 (2014): 3518–24. http://dx.doi.org/10.1002/asia.201402868.

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30

Knorn, Matthias, Eugen Lutsker, and Oliver Reiser. "Isonitriles as supporting and non-innocent ligands in metal catalysis." Chemical Society Reviews 49, no. 21 (2020): 7730–52. http://dx.doi.org/10.1039/d0cs00223b.

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31

Zhang, Yangyang, Qianxiong Zhou, Yue Zheng, et al. "DNA Photocleavage by Non-innocent Ligand-Based Ru(II) Complexes." Inorganic Chemistry 55, no. 9 (2016): 4296–300. http://dx.doi.org/10.1021/acs.inorgchem.6b00028.

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32

Chen, Kun-Hao, Yi-Hung Liu, and Ching-Wen Chiu. "A Non-innocent Ligand Supported Germylene and Its Diverse Reactions." Organometallics 39, no. 24 (2020): 4645–50. http://dx.doi.org/10.1021/acs.organomet.0c00671.

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33

Hall, Michael B. "Intriguing aspects of non-innocent ligands in transition metal complexes." Acta Crystallographica Section A Foundations and Advances 73, a1 (2017): a28. http://dx.doi.org/10.1107/s0108767317099718.

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34

Gantman, Mikhail G., Irina G. Tarkhanova, and Yuri G. Kolyagin. "Non-innocent ligands in copper complexes catalyzed oxidation of thiols." Journal of Sulfur Chemistry 37, no. 5 (2016): 501–14. http://dx.doi.org/10.1080/17415993.2016.1193179.

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35

Allan, Christopher J., Benjamin F. T. Cooper, Hugh J. Cowley, Jeremy M. Rawson, and Charles L. B. Macdonald. "Non-Innocent Ligand Effects on Low-Oxidation-State Indium Complexes." Chemistry - A European Journal 19, no. 43 (2013): 14470–83. http://dx.doi.org/10.1002/chem.201301881.

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36

Smith, Dan A., Andrei S. Batsanov, Karine Costuas, et al. "Exploiting Non-Innocent Ligands to Prepare Masked Palladium(0) Complexes." Angewandte Chemie 122, no. 39 (2010): 7194–98. http://dx.doi.org/10.1002/ange.201003946.

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37

Smith, Dan A., Andrei S. Batsanov, Karine Costuas, et al. "Exploiting Non-Innocent Ligands to Prepare Masked Palladium(0) Complexes." Angewandte Chemie International Edition 49, no. 39 (2010): 7040–44. http://dx.doi.org/10.1002/anie.201003946.

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38

Ringenberg, Mark R., Swarna Latha Kokatam, Zachariah M. Heiden, and Thomas B. Rauchfuss. "Redox-Switched Oxidation of Dihydrogen Using a Non-Innocent Ligand." Journal of the American Chemical Society 130, no. 3 (2008): 788–89. http://dx.doi.org/10.1021/ja076801k.

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39

Marappan, Dinesh, Maadeswaran Palanisamy, Kavitha Velappan, Nirmala Muthukumaran, and Prabusankar Ganesan. "First luminescent triphenyl silanol enabled by non-innocent acridine orange." Inorganic Chemistry Communications 92 (June 2018): 101–5. http://dx.doi.org/10.1016/j.inoche.2018.04.020.

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40

DAS, AMIT, DIPANWITA DAS, TANAYA KUNDU, and GOUTAM KUMAR LAHIRI. "Electronic structures of ruthenium complexes encircling non-innocent ligand assembly." Journal of Chemical Sciences 124, no. 6 (2012): 1181–89. http://dx.doi.org/10.1007/s12039-012-0316-3.

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41

Jach, Franziska, Frank R. Wagner, Zeeshan H. Amber, et al. "Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands." Angewandte Chemie International Edition 60, no. 29 (2021): 15879–85. http://dx.doi.org/10.1002/anie.202103268.

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42

Wang, Yichen, Jing Li, Li Zhang, et al. "Magnetic on–off switching in redox non-innocent ligand bridged binuclear cobalt complexes." Dalton Transactions 47, no. 48 (2018): 17211–15. http://dx.doi.org/10.1039/c8dt04157a.

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43

Piehl, Patrick, Miguel Peña-López, Anna Frey, Helfried Neumann, and Matthias Beller. "Hydrogen autotransfer and related dehydrogenative coupling reactions using a rhenium(i) pincer catalyst." Chemical Communications 53, no. 22 (2017): 3265–68. http://dx.doi.org/10.1039/c6cc09977g.

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44

Lee, Nicholas A., Ken T. Ngo, Gerald E. Gilligan, Massimilliano Lamberto, and Jonathan Rochford. "Non-innocent ligand flavone and curcumin inspired ruthenium photosensitizers for solar energy conversion." Physical Chemistry Chemical Physics 23, no. 31 (2021): 16516–24. http://dx.doi.org/10.1039/d1cp01853a.

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45

Chakraborty, Soumi, Arpan Das, Jasimuddin Ahmed, Sayani Barman, and Swadhin K. Mandal. "Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO2 functionalization." Chemical Communications 56, no. 89 (2020): 13788–91. http://dx.doi.org/10.1039/d0cc05348a.

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46

Vijaykumar, Gonela, Anand Pariyar, Jasimuddin Ahmed, Bikash Kumar Shaw, Debashis Adhikari, and Swadhin K. Mandal. "Tuning the redox non-innocence of a phenalenyl ligand toward efficient nickel-assisted catalytic hydrosilylation." Chemical Science 9, no. 10 (2018): 2817–25. http://dx.doi.org/10.1039/c7sc04687a.

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47

Tahara, Keishiro, Shogo Akehi, Tetsuhiro Akita, Shohei Katao, Jun-ichi Kikuchi, and Ken Tokunaga. "Tuning of intramolecular charge transfer properties and charge distributions in ferrocene-appended catechol derivatives by chemical substitution." Dalton Transactions 44, no. 33 (2015): 14635–45. http://dx.doi.org/10.1039/c5dt01998b.

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48

Smirnov, Andrey S., Luísa M. D. R. S. Martins, Dmitriy N. Nikolaev, et al. "Structure and catalytic properties of novel copper isatin Schiff base complexes." New Journal of Chemistry 43, no. 1 (2019): 188–98. http://dx.doi.org/10.1039/c8nj02718h.

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49

Mathew, J., Y. Nakajima, Y. K. Choe, et al. "Olefin hydrosilylation catalyzed by cationic nickel(ii) allyl complexes: a non-innocent allyl ligand-assisted mechanism." Chemical Communications 52, no. 40 (2016): 6723–26. http://dx.doi.org/10.1039/c6cc01665k.

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50

Duarte, Gabriel M., Jason D. Braun, Patrick K. Giesbrecht, and David E. Herbert. "Redox non-innocent bis(2,6-diimine-pyridine) ligand–iron complexes as anolytes for flow battery applications." Dalton Transactions 46, no. 47 (2017): 16439–45. http://dx.doi.org/10.1039/c7dt03915h.

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