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Journal articles on the topic 'Manganese carbonyl'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Martínez-Ferraté, Oriol, Basujit Chatterjee, Christophe Werlé, and Walter Leitner. "Hydrosilylation of carbonyl and carboxyl groups catalysed by Mn(i) complexes bearing triazole ligands." Catalysis Science & Technology 9, no. 22 (2019): 6370–78. http://dx.doi.org/10.1039/c9cy01738k.

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2

Li, Guoliang, Limei Wen, and R. Bruce King. "Heterobimetallic Chromium Manganese Carbonyl Nitrosyls: Comparison with Isoelectronic Homometallic Binuclear Chromium Carbonyl Nitrosyls and Manganese Carbonyls." Inorganics 7, no. 10 (2019): 127. http://dx.doi.org/10.3390/inorganics7100127.

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The heterometallic chromium-manganese carbonyl nitrosyls CrMn(NO)(CO)n (n = 9, 8) have been investigated by density functional theory. The lowest energy CrMn(NO)(CO)9 structures have unbridged staggered conformations with a ~2.99 Å Cr–Mn single bond similar to the experimental and lowest energy structures of the isoelectronic Mn2(CO)10 and Cr2(NO)2(CO)8. A significantly higher energy CrMn(NO)(CO)9 isomer has a nearly symmetrical bridging nitrosyl group and a very weakly semibridging carbonyl group. The two lowest energy structures of the unsaturated CrMn(NO)(CO)8 have a five-electron donor bri

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3

Wang, Hongyan, Yaoming Xie, R. Bruce King, and Henry F. Schaefer. "Manganese Carbonyl Nitrosyls: Comparison with Isoelectronic Iron Carbonyl Derivatives." Inorganic Chemistry 45, no. 26 (2006): 10849–58. http://dx.doi.org/10.1021/ic0616939.

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4

Wang, Hongyan, Yaoming Xie, Jun D. Zhang, R. Bruce King, and Henry F. Schaefer. "Chromium Carbonyl Nitrosyls: Comparison with Isoelectronic Manganese Carbonyl Derivatives." Inorganic Chemistry 46, no. 5 (2007): 1836–46. http://dx.doi.org/10.1021/ic0620541.

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5

Almutairi, Nora, Srikanth Vijjamarri, and Guodong Du. "Manganese Salan Complexes as Catalysts for Hydrosilylation of Aldehydes and Ketones." Catalysts 13, no. 4 (2023): 665. http://dx.doi.org/10.3390/catal13040665.

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Manganese has attracted significant recent attention due to its abundance, low toxicity, and versatility in catalysis. In the present study, a series of manganese (III) complexes supported by salan ligands have been synthesized and characterized, and their activity as catalysts in the hydrosilylation of carbonyl compounds was examined. While manganese (III) chloride complexes exhibited minimal catalytic efficacy without activation of silver perchlorate, manganese (III) azide complexes showed good activity in the hydrosilylation of carbonyl compounds. Under optimized reaction conditions, severa

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6

Wadayama, Kosei, Tsugiko Takase, and Dai Oyama. "Selective synthesis and crystal structures of manganese(I) complexes with a bi- or tridentate terpyridine ligand." Acta Crystallographica Section E Crystallographic Communications 76, no. 7 (2020): 1139–42. http://dx.doi.org/10.1107/s2056989020008178.

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The crystal structures of two manganese(I) complexes with a different coordination mode of the supporting ligand are reported: fac-bromidotricarbonyl(4′-phenyl-2,2′:6′,2′′-terpyridine-κ2 N,N′)manganese(I), [MnBr(C21H15N3)(CO)3], I, and cis-bromidodicarbonyl(4′-phenyl-2,2′:6′,2′′-terpyridine-κ3 N,N′,N′′)manganese(I), [MnBr(C21H15N3)(CO)2], II. In both complexes, the manganese(I) atom is coordinated by terminal carbonyl ligands, a bromide ion, and a 4′-phenyl-2,2′:6′,2′′-terpyridine ligand within a distorted octahedral environment. In I, the metal ion is facially coordinated by three carbonyl li

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7

Adams, Richard D., O.-Sung Kwon, and Shaobin Miao. "Disulfido Metal Carbonyl Complexes Containing Manganese." Accounts of Chemical Research 38, no. 3 (2005): 183–90. http://dx.doi.org/10.1021/ar0402457.

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8

Kreiter, Cornelius G., та Klaus Lehr. "Photochemische Reaktionen von Übergangsmetall-Organyl-Komplexen mit Olefnen, VI. Reaktionen von Tricarbonyl-η5-2,4-cyclohexadienyl-mangan mit konjugierten Dienen / Photochemical Reactions of Transition Metal Organyl Complexes with Olefins, VI. Reactions of Tricarbonyl (η5-2,4-cyclohexadienyl)manganese with Conjugated Dienes". Zeitschrift für Naturforschung B 46, № 10 (1991): 1377–83. http://dx.doi.org/10.1515/znb-1991-1016.

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Tricarbonyl-η5-2,4-cyclohexadien-1-yl-manganese (1) was reacted photochemically at 253 K with simple conjugated dienes. Four different types of products were obtained, depending upon the dienes. With 1,3-butadiene (A) dicarbonyl-η4:3-1-(3-buten-1,2-diyl)-2,4-cyclohexadiene-manganese (2A) is isolated. 2-Methyl-1,3-butadiene (B) yields the methyl-substituted diastereomeric dicarbonyls 2B, 2B′, the [4+5]-cycloadduct tricarbonyl-η3:2-3-methyl-bicyclo-[4.3.1]-3,8-decadien-7-yl-manganese (3B) and tetracarbonyl-η3-4-methylene-bicyclo[4.3.1]-8-decen-3-yl-manganese (4B) with an exocyclically coordinate

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9

Kanno, Takatoshi, Tsugiko Takase та Dai Oyama. "Synthesis and crystal structures of manganese(I) carbonyl complexes bearing ester-substituted α-diimine ligands". Acta Crystallographica Section E Crystallographic Communications 76, № 9 (2020): 1433–36. http://dx.doi.org/10.1107/s2056989020010750.

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The crystal structures of two manganese(I) complexes with ester-substituted bipyridine or biquinoline supporting ligands are reported, namely, fac-bromidotricarbonyl(diethyl 2,2′-bipyridine-4,4′-dicarboxylate-κ2 N,N′)manganese(I), [MnBr(C16H16N2O4)(CO)3], I, and fac-bromidotricarbonyl(diethyl 2,2′-biquinoline-4,4′-dicarboxylate-κ2 N,N′)manganese(I), [MnBr(C24H20N2O4)(CO)3], II. In both complexes, the manganese(I) atom adopts a distorted octahedral coordination sphere defined by three carbonyl C atoms, a Br− anion and two N atoms from the chelating α-diimine ligand. Both complexes show fac conf

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10

Fohlmeister, Lea, and Cameron Jones. "Stabilisation of carbonyl free amidinato-manganese(ii) hydride complexes: “masked” sources of manganese(i) in organometallic synthesis." Dalton Transactions 45, no. 4 (2016): 1436–42. http://dx.doi.org/10.1039/c5dt04504e.

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The first carbonyl free amidinato-manganese(ii) hydride complexes have been prepared (see picture). Preliminary reactivity studies reveal that one of the complexes acts as a “masked” source of an amidinato-manganese(i) fragment in its reactions.

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11

Hou, Kaipeng, Sherman J. L. Lauw, Richard D. Webster, and Wai Yip Fan. "Electrochemical proton reduction catalysed by selenolato-manganese carbonyl complexes." RSC Advances 5, no. 49 (2015): 39303–9. http://dx.doi.org/10.1039/c5ra04432d.

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12

Dou, Na, Bin Peng, Qian-shu Li, et al. "Disulfide ligands and sulfur-bridging carbonyls: Remarkable examples in manganese carbonyl chemistry." Polyhedron 52 (March 2013): 1375–84. http://dx.doi.org/10.1016/j.poly.2012.05.023.

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13

Poh, Hwa Tiong, Tsz Sian Chwee, and Wai Yip Fan. "Stable manganese carbonyl radicals as a rapid colorimetric thiol and hydrazine sensor." RSC Advances 5, no. 20 (2015): 15159–63. http://dx.doi.org/10.1039/c4ra16483k.

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14

Amorim, André L., Marcos M. Peterle, Ana Guerreiro, et al. "Synthesis, characterization and biological evaluation of new manganese metal carbonyl compounds that contain sulfur and selenium ligands as a promising new class of CORMs." Dalton Transactions 48, no. 17 (2019): 5574–84. http://dx.doi.org/10.1039/c9dt00616h.

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15

Masters, A. P., M. Parvez, T. S. Sorensen та F. Sun. "Organometallic products from the reaction of the isoelectronic Mn(CO)5− and Cr(CO)4NO− metallate anions with bis-α-bromocyclopropyl ketone". Canadian Journal of Chemistry 71, № 2 (1993): 230–38. http://dx.doi.org/10.1139/v93-034.

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Mn(CO)5− and Cr(CO)4NO− react with the title ketone to give organometallic products. In the chromium case, a single metallofuran product is produced. In the manganese reaction, one can isolate a series of four complexes, two of which have a structure closely related to the chromium complex. The other two complexes are assigned an acyl manganese structure. The structures of the chromium complex and one of the acyl manganese complexes have been determined by X-ray methods. One finds a distorted octahedral bonding about the metal atom in each case. The chromium complex has bond lengths very simil

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16

Waiba, Satyadeep, Sayan K. Jana, Ayan Jati, Akash Jana та Biplab Maji. "Manganese complex-catalysed α-alkylation of ketones with secondary alcohols enables the synthesis of β-branched carbonyl compounds". Chemical Communications 56, № 60 (2020): 8376–79. http://dx.doi.org/10.1039/d0cc01460e.

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17

Li, Jiajia, Andrew Kerr, Satu Häkkinen, et al. "Manganese carbonyl induced cationic reversible addition–fragmentation chain transfer (C-RAFT) polymerization under visible light." Polymer Chemistry 11, no. 15 (2020): 2724–31. http://dx.doi.org/10.1039/c9py01785b.

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18

Li, Huidong, Hao Feng, Weiguo Sun, et al. "Binuclear pentalene manganese carbonyl complexes: conventionaltransand unconventionalcisstructures." Molecular Physics 110, no. 15-16 (2012): 1637–50. http://dx.doi.org/10.1080/00268976.2012.663942.

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19

Deng, Jianming, Qian-shu Li, Yaoming Xie, and R. Bruce King. "Manganese carbonyl fluorides: are they viable molecules?" Dalton Transactions 41, no. 20 (2012): 6225. http://dx.doi.org/10.1039/c2dt30405h.

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20

Sinopoli, Alessandro, Nathan T. La Porte, Jose F. Martinez, Michael R. Wasielewski, and Muhammad Sohail. "Manganese carbonyl complexes for CO 2 reduction." Coordination Chemistry Reviews 365 (June 2018): 60–74. http://dx.doi.org/10.1016/j.ccr.2018.03.011.

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21

Connelly, Neil G., Stephen J. Raven, Gabino A. Carriedo, and Victor Riera. "Redox-catalysed isomerisation of manganese carbonyl derivatives." Journal of the Chemical Society, Chemical Communications, no. 13 (1986): 992. http://dx.doi.org/10.1039/c39860000992.

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22

Du, Jing, Zhong-Ling Lang, Yuan-Yuan Ma, et al. "Polyoxometalate-based electron transfer modulation for efficient electrocatalytic carbon dioxide reduction." Chemical Science 11, no. 11 (2020): 3007–15. http://dx.doi.org/10.1039/c9sc05392a.

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23

Pignon, Antoine, Erwan Le Gall, and Thierry Martens. "A new manganese-mediated, cobalt-catalyzed three-component synthesis of (diarylmethyl)sulfonamides." Beilstein Journal of Organic Chemistry 10 (February 17, 2014): 425–31. http://dx.doi.org/10.3762/bjoc.10.39.

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The synthesis of (diarylmethyl)sulfonamides and related compounds by a new manganese-mediated, cobalt-catalyzed three-component reaction between sulfonamides, carbonyl compounds and organic bromides is described. This organometallic Mannich-like process allows the formation of the coupling products within minutes at room temperature. A possible mechanism, emphasizing the crucial role of manganese is proposed.

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24

Azadbakht, Reza, Abbas Amini Manesh, Mahdieh Malayeri, and Behzad Dehghani. "Synthesis, characterization, reactivity and catalytic activity of a novel chiral manganese Schiff base complex." New Journal of Chemistry 39, no. 8 (2015): 6459–64. http://dx.doi.org/10.1039/c5nj01031d.

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25

Smith, Charlotte L., Rob Clowes, Reiner Sebastian Sprick, Andrew I. Cooper, and Alexander J. Cowan. "Metal–organic conjugated microporous polymer containing a carbon dioxide reduction electrocatalyst." Sustainable Energy & Fuels 3, no. 11 (2019): 2990–94. http://dx.doi.org/10.1039/c9se00450e.

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26

Ren, Qing-Gang, Xian-Tai Zhou, and Hong-Bing Ji. "Biomimetic models of nitric oxide synthase for the oxidation of oximes to carbonyl compounds catalyzed by water-soluble manganese porphyrins in aqueous solution." Journal of Porphyrins and Phthalocyanines 15, no. 03 (2011): 211–16. http://dx.doi.org/10.1142/s1088424611003173.

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A mild green and efficient approach for hydrogen peroxide oxidative converting oximes to the corresponding carbonyl compounds with a water-soluble manganese porphyrin as catalyst in water/acetone mixture has been developed. The water-soluble manganese porphyrin showed an excellent activity for the oxidative deoximation reactions of various oximes under ambient conditions in the absence of any additive. The oxidative deoximation was through the formation of high valent oxo-manganese species, which was confirmed by in situ UV-vis spectroscopy.

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27

Beltrán, Tomás F., Guillermo Zaragoza, and Lionel Delaude. "Mono- and bimetallic manganese–carbonyl complexes and clusters bearing imidazol(in)ium-2-dithiocarboxylate ligands." Dalton Transactions 46, no. 6 (2017): 1779–88. http://dx.doi.org/10.1039/c6dt04780g.

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28

Obaleye, Joshua A., and Olufunso O. Abosede. "Synthesis, characterization and antibacterial susceptibility testing of manganese complexes of doxycyline with bipyridine and phenanthroline." Ovidius University Annals of Chemistry 30, no. 2 (2019): 70–74. http://dx.doi.org/10.2478/auoc-2019-0013.

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Abstract Three manganese complexes of the antibiotic doxycyline viz.: manganese doxycyline, [MnDox2]Cl2‧2H2O (1), and manganese doxycyline with bipyridine, [MnDox2(bpy)]Cl2‧8H2O (2), and phenanthroline, [MnDox2(phen)]Cl2‧8H2O (3), as the ancillary ligand were synthesized and characterized by FT-IR, elemental analysis and electrospray mass spectroscopy. The three complexes show good solubility in DMF and DMSO. Data obtained from spectroscopic techniques used show that doxycycline coordinates to the central manganese atom through the oxygen of the amide group and the carbonyl oxygen atom of ring

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29

Eastwood, Jonathan B., L. Anders Hammarback, Matthew T. McRobie, et al. "Correction: Time-resolved infra-red spectroscopy reveals competitive water and dinitrogen coordination to a manganese(i) carbonyl complex." Dalton Transactions 49, no. 21 (2020): 7267. http://dx.doi.org/10.1039/d0dt90086a.

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Correction for ‘Time-resolved infra-red spectroscopy reveals competitive water and dinitrogen coordination to a manganese(i) carbonyl complex’ by Jonathan B. Eastwood et al., Dalton Trans., 2020, DOI: 10.1039/c9dt04878b.

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30

Van der Maelen Uría, Juan F., Javier Ruiz, and Santiago García-Granda. "Theoreticalversusexperimental geometries in S-bridged manganese carbonyl complexes." Journal of Applied Crystallography 36, no. 4 (2003): 1050–55. http://dx.doi.org/10.1107/s0021889803010276.

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The experimental geometry obtained from single-crystal X-ray diffraction for a number of binuclear S-bridged manganese complexes is compared with the results of theoretical calculations made at theab initiolevel by using Hartree–Fock and density functional theory methods with medium-size and large basis sets. The optimized geometries obtained were somewhat relaxed when compared with the experimental ones, with very similar bond and torsion angles but longer bond lengths. The mean square deviation for bond lengths (angles) was found to be between 0.046 Å (1.1°) and 0.004 Å (0.7°) depending on t

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31

Trovitch, Ryan J. "The Emergence of Manganese-Based Carbonyl Hydrosilylation Catalysts." Accounts of Chemical Research 50, no. 11 (2017): 2842–52. http://dx.doi.org/10.1021/acs.accounts.7b00422.

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32

Aucott, Benjamin J., Anne-Kathrin Duhme-Klair, Benjamin E. Moulton, et al. "Manganese Carbonyl Compounds Reveal Ultrafast Metal–Solvent Interactions." Organometallics 38, no. 11 (2019): 2391–401. http://dx.doi.org/10.1021/acs.organomet.9b00212.

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33

Carriedo, G. A., V. Riera, M. L. Rodríguez, and J. J. Sainz-Velicia. "Cationic carbonyl complexes of manganese(I) with diphenylphosphine." Polyhedron 6, no. 10 (1987): 1879–84. http://dx.doi.org/10.1016/s0277-5387(00)81099-2.

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34

Herrick,, R. S. "Flash Photolysis Studies of Dinuclear Manganese Carbonyl Compounds." Reviews in Inorganic Chemistry 8, no. 1-2 (1986): 1–30. http://dx.doi.org/10.1515/revic.1986.8.1-2.1.

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35

Lü, Wenjun, Chaoyang Wang, Qiong Luo, et al. "Carbonyl migration from phosphorus to the metal in binuclear phosphaketenyl metal carbonyl complexes to give bridging diphosphido complexes." New Journal of Chemistry 39, no. 2 (2015): 1390–403. http://dx.doi.org/10.1039/c4nj01311e.

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Carbonyl groups from bridging phosphaketenyl ligands in Mn<sub>2</sub>(CO)<sub>8</sub>(μ-PCO)<sub>2</sub> are predicted to migrate from phosphorus to manganese upon decarbonylation, giving the diphosphido Mn<sub>2</sub>(CO)<sub>n+2</sub>(μ-P<sub>2</sub>) derivatives.

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36

Kochergin, V. K., R. A. Manzhos, and A. G. Krivenko. "One-Step Plasma-Assisted Electrochemical Synthesis of Nanocomposites of Few-Layer Graphene Structures with Manganese Oxides as Electrocatalysts for Oxygen Reduction Reaction." Электрохимия 59, no. 4 (2023): 225–34. http://dx.doi.org/10.31857/s0424857023040096.

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Using the method of plasma-assisted electrochemical exfoliation of graphite, a nanocomposite, which consists of few-layer graphene structures with surface decorated with manganese oxides nanoparticles, is synthesized in one-step process. It is found that this material exhibits a high electrocatalytic activity towards the oxygen reduction reaction due to the presence of manganese in the +2 and +3 oxidation states, and also carbonyl (quinone) functional groups on the surface of graphene structures.

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37

Connor, Joseph A., and Andreas Göbel. "Thermochemistry of thiolato derivatives of manganese carbonyl. The strength of manganese-sulphur bonds." Polyhedron 14, no. 20-21 (1995): 3107–10. http://dx.doi.org/10.1016/0277-5387(95)00085-7.

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38

Liu, Xian-mei, Chao-yang Wang, Qian-shu Li, Yaoming Xie, R. Bruce King, and Henry F. Schaefer III. "Mononuclear and binuclear manganese carbonyl hydrides: the preference for bridging hydrogens over bridging carbonyls." Dalton Transactions, no. 19 (2009): 3774. http://dx.doi.org/10.1039/b822913a.

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39

Jia, Jiage, Yanhui Zhang, Panpan Zhang, et al. "Synthesis and characterization of a series of novel polyoxometalate-supported carbonyl manganese derivatives." RSC Advances 6, no. 110 (2016): 108335–42. http://dx.doi.org/10.1039/c6ra23547f.

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A series of novel heteropolytungstates-supported carbonyl manganese derivatives have been synthesized, which are the first examples of grafting [Mn(CO)<sub>3</sub>]<sup>+</sup> moieties and Mn<sup>2+</sup> on the tungsto-antimonates/bismutates.

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40

Machan, Charles W., and Clifford P. Kubiak. "Electrocatalytic reduction of carbon dioxide with Mn(terpyridine) carbonyl complexes." Dalton Transactions 45, no. 43 (2016): 17179–86. http://dx.doi.org/10.1039/c6dt03243e.

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The behavior of a series of Manganese (Mn) carbonyl compounds with 2,2′:6′,2′′-terpyridine (tpy) in κ<sup>2</sup>-N,N′ and κ<sup>3</sup>-N,N′,N′′ coordination modes under electrochemically reducing conditions is reported.

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41

Carrington, Samantha J., Indranil Chakraborty, and Pradip K. Mascharak. "Exceptionally rapid CO release from a manganese(i) tricarbonyl complex derived from bis(4-chloro-phenylimino)acenaphthene upon exposure to visible light." Dalton Transactions 44, no. 31 (2015): 13828–34. http://dx.doi.org/10.1039/c5dt01007a.

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Both in solid state and in solution, the manganese carbonyl complex [MnBr(CO)<sub>3</sub>(BIAN)] rapidly releases CO upon illumination with visible light. This complex could find use in delivery of rapid flux of CO to biological targets.

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42

Mansour, Ahmed M., and Alexandra Friedrich. "IClick cycloaddition reaction of light-triggered manganese(i) carbonyl complexes." New Journal of Chemistry 42, no. 22 (2018): 18418–25. http://dx.doi.org/10.1039/c8nj01838c.

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43

Schmitt, Georg, H. Pritzkow, and H. P. Latscha. "Bisdisubstituierte aromatische Phosphane als Komplexliganden / Bisdisubstituted Aromatic Phosphanes as Ligands for Metal Complexes." Zeitschrift für Naturforschung B 42, no. 9 (1987): 1115–20. http://dx.doi.org/10.1515/znb-1987-0911.

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The photochemical reaction of o-C6H4(PR2)2; R = OCH3, OC2H5 , m-C6H4(PR2)2; R = N(CH3): and p-C6H4(PR2)2; R = OCH3. N(CH3)2 with (tricarbonylj(methylcyclopentadienyl)- manganese (Cp')Mn(CO)3 (6) and p-C6H4(P(N(CHO3)2)2)2 with (tricarbonyl)(methyl)(cyclopenta- dienyl)molybdenum (CH3)(Cp)Mo(CO)3 (7) yields new manganese and molybdenum complexes. o-Phenylen-bis(phosphonousaciddimethylester)(carbonyl)(methylcyclopentadienyl )manganese (8) forms yellow crystals, whose structure is reported. The reaction of o-C6H4(P(OCH3)2)2 (1) with NiCl2 gives a 1:1 phosphane complex (14). Ni(OH)Clopm. The complex

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44

Hoque, Md Anwarul, Md Arzu Miah, Md Nurul Abser, Abul K. Azad, Kamrun N. Khan, and Md Manzurul Karim. "Binuclear Rhenium and Manganese Carbonyl Compounds Containing Hetero-Mercaptanes." Journal of the Bangladesh Chemical Society 25, no. 1 (2012): 62–70. http://dx.doi.org/10.3329/jbcs.v25i1.11775.

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Treatment of 2-Mercaptothiazoline, 2-Mercaptobenzimidazole, 2-Mercapto-1- methylimidazole with [M2(CO)10] (M = Re and Mn) at ambient temperature in presence of decarbonylating reagent Me3NO give the complexes [Mn2(?-?2-C3H4NS2)2(CO)6] (1), [Re2(?-?2-C3H4NS2)2(CO)6] (2), [Mn2(?-?2-C7H5SN2)2(CO)6] (3), [Re2(?-?2- C7H5SN2)2(CO)6] (4), [Re2(?-?2-C4H5N2S)2(CO)6] (5) and [Re2(?1-C4H5N2SH)(CO)9] (6) respectively. All the compounds have been characterized by IR, 1H NMR and mass spectral data. The heterocyclic ligands are expected to be coordinated to two or single metal atom through the nitrogen and s

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45

Chardon, Sylvie. "Manganese-Carbonyl Complexes As Catalysts for CO2 Electrochemical Reduction." ECS Meeting Abstracts MA2020-01, no. 36 (2020): 1517. http://dx.doi.org/10.1149/ma2020-01361517mtgabs.

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46

Shieh, Minghuey, and Miao-Hsing Hsu. "Chalcogen-Containing Manganese Carbonyl Clusters: Synthesis and Structural Transformations." Journal of Cluster Science 15, no. 2 (2004): 91–106. http://dx.doi.org/10.1023/b:jocl.0000027395.39228.01.

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47

Gregg, Brian T., and Alan R. Cutler. "Manganese Carbonyl Bromide-Catalyzed Alcoholysis of the Monohydrosilane HSiMe2Ph." Organometallics 13, no. 3 (1994): 1039–43. http://dx.doi.org/10.1021/om00015a043.

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48

Herrick, Richard S., Thomas R. Herrinton, Howard W. Walker, and Theodore L. Brown. "Rates of halogen atom transfer to manganese carbonyl radicals." Organometallics 4, no. 1 (1985): 42–45. http://dx.doi.org/10.1021/om00120a008.

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Motz, Philip L., John J. Alexander, and Charles F. Campana. "Reactions of an imidoyl halide with manganese carbonyl complexes." Journal of Organometallic Chemistry 379, no. 1-2 (1989): 119–27. http://dx.doi.org/10.1016/0022-328x(89)80031-2.

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Demir, Ayhan S., Cihangir Tanyeli, and Ertan Altinel. "Manganese triacetate mediated regeneration of carbonyl compounds from oximes." Tetrahedron Letters 38, no. 41 (1997): 7267–70. http://dx.doi.org/10.1016/s0040-4039(97)01688-2.

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