Category: 14516-54-2

《Chemoselective semihydrogenation of alkynes catalyzed by manganese(I)-PNP pincer complexes》 was written by Garbe, Marcel; Budweg, Svenja; Papa, Veronica; Wei, Zhihong; Hornke, Helen; Bachmann, Stephan; Scalone, Michelangelo; Spannenberg, Anke; Jiao, Haijun; Junge, Kathrin; Beller, Matthias. Category: bromides-buliding-blocks And the article was included in Catalysis Science & Technology in 2020. The article conveys some information:

A general manganese catalyzed chemoselective semihydrogenation of alkynes R1CCR2 (R1 = Ph, 4-bromophenyl, 4-methoxyphenyl, 4-[methoxy(oxo)methane]phenyl, etc.; R2 = Ph, 4-chlorophenyl, 2-amino-5-chlorophenyl, pyridin-3-yl, etc.) to olefins R1HC=CHR2 in the presence of mol. hydrogen is described. The best results are obtained by applying the aliphatic Mn PNP pincer complex Mn-3c which allows the transformation of various substituted internal alkynes to the resp. Z-olefins under mild conditions and in high yields. Mechanistic investigations based on experiments and computations indicate the formation of the Z-isomer via an outer-sphere mechanism. In addition to this study using Bromopentacarbonylmanganese(I), there are many other studies that have used Bromopentacarbonylmanganese(I)(cas: 14516-54-2Category: bromides-buliding-blocks) was used in this study.

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《fac-Bis(phenoxatellurine) tricarbonyl manganese(I) bromide》 was written by Mostaghimi, Farzin; Lork, Enno; Beckmann, Jens. Electric Literature of C5BrMnO5 And the article was included in Main Group Metal Chemistry in 2020. The article conveys some information:

The reaction of (CO)5MnBr with phenoxatellurine (PT) provided the octahedral complex fac-(CO)3(PT)2MnBr in which the two PT ligands are situated in cis-position. The experimental part of the paper was very detailed, including the reaction process of Bromopentacarbonylmanganese(I)(cas: 14516-54-2Electric Literature of C5BrMnO5)

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Electric Literature of C5BrMnO5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Jayaprakash, Harikrishnan published an article in 2021. The article was titled 《Mn(I) phosphine-amino-phosphinites: a highly modular class of pincer complexes for enantioselective transfer hydrogenation of aryl-alkyl ketones》, and you may find the article in Dalton Transactions.Name: Bromopentacarbonylmanganese(I) The information in the text is summarized as follows:

A series of Mn(I) catalysts with readily accessible and more π-accepting phosphine-amino-phosphinite (P'(O)N(H)P) pincer ligands have been explored for the asym. transfer hydrogenation of aryl-alkyl ketones which led to good to high enantioselectivities (up to 98%) compared to other reported Mn-based catalysts for such reactions. The easy tunability of the chiral backbone and the phosphine moieties makes P'(O)N(H)P an alternative ligand framework to the well-known PNP-type pincers.Bromopentacarbonylmanganese(I)(cas: 14516-54-2Name: Bromopentacarbonylmanganese(I)) was used in this study.

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Name: Bromopentacarbonylmanganese(I)

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Safety of Bromopentacarbonylmanganese(I)In 2022 ,《Synthesis and properties of a new nine-membered triphospha-macrocyclic complex via a manganese(I) tricarbonyl template》 appeared in Journal of Molecular Structure. The author of the article were Zhang, Wenjian; Levason, William; Reid, Gillian. The article conveys some information:

Reaction of the primary diphosphine H2P(CH2)2PH2 with [MnBr(CO)5], followed by removal of the bromide by treatment with AgOTf (OTf = CF3SO3) and addition of PAr3 (Ar = o-C6H4F), gives the acyclic precursor complex, fac-[Mn(CO)3{H2P(CH2)2PH2}(PAr3)][OTf], thus positioning the primary phosphine functions adjacent to the o-fluorophenyl substituents. The identity of this species was confirmed by multinuclear NMR (1H, 19F{1H}, 31P{1H} and 55Mn) and IR spectroscopic anal., as well as from a single crystal x-ray anal. Subsequent treatment of this complex with KOtBu (potassium tertiary butoxide) causes a double P-C coupling reaction, with defluorination of two aryl groups, and gives a nine-membered triphosphine macrocyclic complex. Methylation (KOtBu/MeI) of the two remaining secondary phosphine function yields the complex [Mn(CO)3(1)][OTf], which was characterized similarly by multinuclear NMR and IR spectroscopy, and by electrospray mass spectrometry. A single crystal x-ray structure determination confirms the distorted octahedral coordination at Mn(I), with the triphosphine macrocycle occupying three mutually facial coordination sites. As expected, this complex is extremely thermodynamically stable and kinetically inert, being unaffected by prolonged refluxing with either Me3NO or thiophenolate in MeCN. After reading the article, we found that the author used Bromopentacarbonylmanganese(I)(cas: 14516-54-2Safety of Bromopentacarbonylmanganese(I))

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Safety of Bromopentacarbonylmanganese(I)

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《Manganese(I) κ2-NN complex-catalyzed formic acid dehydrogenation》 was written by Leval, Alexander; Junge, Henrik; Beller, Matthias. Reference of Bromopentacarbonylmanganese(I) And the article was included in Catalysis Science & Technology in 2020. The article conveys some information:

Hydrogen use as a sustainable energy vector is of growing interest and is the subject of current intensive research. We report herein an upgraded follow-up system for formic acid (FA) dehydrogenation (DH) catalyzed by [Mn(BisIm)(CO)3Br] (BisIm = 4,4′,5,5′-tetrahydro-1H,1′H-2,2′-bisimidazole). The latter belongs to a family of novel catalysts we developed, which are interesting since they bear easily accessible ligands from cheap, com. available starting materials. The novel catalyst system allows for improved hydrogen generation and better catalyst turnover numbers (7883 after 12 cycles of FA dosage). In addition, a significantly lower CO content in the gas phase was also achieved (47 ppm). Extended investigation of the influence of the ligand structure on the catalytic performances confirmed that the non-bonding electron pair on the N-H moiety, on the 3rd position of each imidazoline ring, is crucial for the transformation. The experimental process involved the reaction of Bromopentacarbonylmanganese(I)(cas: 14516-54-2Reference of Bromopentacarbonylmanganese(I))

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Reference of Bromopentacarbonylmanganese(I)

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Zhang, Hai-Lin; Yu, Ya-Ting; Wang, Yi; Tang, Qi; Yang, Shi-Ping; Liu, Jin-Gang published an article in 2021. The article was titled 《Visible light-controlled carbon monoxide delivery combined with the inhibitory activity of histone deacetylases from a manganese complex for an enhanced antitumor therapy》, and you may find the article in Journal of Inorganic Biochemistry.Synthetic Route of C5BrMnO5 The information in the text is summarized as follows:

Multifunctional drugs with synergistic effects have been widely developed to enhance the treatment efficiency of various diseases, such as malignant tumors. Herein, a novel bifunctional manganese(I)-based prodrug [MnBr(CO)3(APIPB)] (APIPB = N-(2-aminophen-yl)-4-(1H-imidazo[4,5-f] [1, 10] phenanthrolin-2-yl)benzamide) with inhibitory histone deacetylase (HDAC) activity and light-controlled carbon monoxide (CO) delivery was successfully designed and synthesized. [MnBr(CO)3(APIPB)] readily released CO under visible light irradiation (λ > 400 nm) through which the amount of released CO could be controlled by manipulating light power d. and illumination time. In the absence of light irradiation, the cytotoxic effect of [MnBr(CO)3(APIPB)] on cancer cells was greater than that of the com. available HDAC inhibitor MS-275. Consequently, with a combination of CO delivery and HDAC inhibitory activity, [MnBr(CO)3(APIPB)] showed a remarkably enhanced antitumor effect on HeLa cells (IC50 = 3.2μM) under visible light irradiation Therefore, this approach shows potential for the development of medicinal metal complexes for combined antitumor therapies. In the experimental materials used by the author, we found Bromopentacarbonylmanganese(I)(cas: 14516-54-2Synthetic Route of C5BrMnO5)

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Synthetic Route of C5BrMnO5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Formula: C5BrMnO5In 2020 ,《In Situ Solution-State Characterization of MOF-Immobilized Transition-Metal Complexes by Infrared Spectroscopy》 was published in ACS Applied Materials & Interfaces. The article was written by Mamlouk, Hind; Elumalai, Palani; Kumar, Manyam Praveen; Aidoudi, Farida H.; Bengali, Ashfaq A.; Madrahimov, Sherzod T.. The article contains the following contents:

Transition metal catalysts immobilized on the surface of MOFs, are being utilized for an ever increasing number of reactions ranging from couplings to olefin oligomerization. While these reactions are usually performed in solution, unlike their homo-geneous counterparts, the insolubility of the MOF systems makes it difficult to obtain detailed mechanistic information by in situ spectroscopic anal. in solution In this report, we present a synthetic method to solubilize these systems by grafting oligomers on the surface of the MOF particles, making it possible to characterize these species by transmission IR spectros-copy. The fundamental photochem. of these catalysts was also studied and compared to that of their homogeneous counterparts. This work establishes a proof of principle for in solution monitoring of heterogeneous catalysts. In the part of experimental materials, we found many familiar compounds, such as Bromopentacarbonylmanganese(I)(cas: 14516-54-2Formula: C5BrMnO5)

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Formula: C5BrMnO5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《N-Heterocyclic Silylenes as Ligands in Transition Metal Carbonyl Chemistry: Nature of Their Bonding and Supposed Innocence》 was published in Chemistry – A European Journal in 2020. These research results belong to Krahfuss, Mirjam J.; Nitsch, Joern; Bickelhaupt, F. Matthias; Marder, Todd B.; Radius, Udo. Computed Properties of C5BrMnO5 The article mentions the following:

A study on the reactivity of the N-heterocyclic silylene Dipp2NHSi (1,3-bis(diisopropylphenyl)-1,3-diaza-2-silacyclopent-4-en-2-ylidene) with the transition metal complexes [Ni(CO)4], [M(CO)6] (M = Cr, Mo, W), [Mn(CO)5(Br)] and [(η5-C5H5)Fe(CO)2(I)] is reported. N-heterocyclic silylenes, the higher homologs of the now ubiquitous NHC ligands, show a remarkably different behavior in coordination chem. compared to NHC ligands. Calculations on the electronic features of these ligands revealed significant differences in the frontier orbital region which lead to some peculiarities of the coordination chem. of silylenes, as demonstrated by the synthesis of the dinuclear, NHSi-bridged complex [{Ni(CO)2(μ-Dipp2NHSi)}2] (2), complexes [M(CO)5(Dipp2NHSi)] (M = Cr 3, Mo 4, W 5), [Mn(CO)3(Dipp2NHSi)2(Br)] (9) and [(η5-C5H5)Fe(CO)2(Dipp2NHSi-I)] (10). DFT calculations on several model systems [Ni(L)], [Ni(CO)3(L)], and [W(CO)5(L)] (L = NHC, NHSi) reveal that carbenes are typically the much better donor ligands with a larger intrinsic strength of the metal-ligand bond. The decrease going from the carbene to the silylene ligand is mainly caused by favorable electrostatic contributions for the NHC ligand to the total bond strength, whereas the orbital interactions were often found to be higher for the silylene complexes. Also, the contribution of σ- and π-interaction depends significantly on the system under study. The σ-interaction is often much weaker for the NHSi ligand compared to NHC but the π-interaction prevails for many NHSi complexes. For the carbonyl complexes, the NHSi ligand is the better σ-donor ligand, and contributions of π-symmetry play only a minor role for the NHC and NHSi co-ligands.Bromopentacarbonylmanganese(I)(cas: 14516-54-2Computed Properties of C5BrMnO5) was used in this study.

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Computed Properties of C5BrMnO5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《Cytotoxicity of Mn-based photoCORMs of ethynyl-α-diimine ligands against different cancer cell lines: The key role of CO-depleted metal fragments》 was written by Rossier, Jeremie; Delasoie, Joachim; Haeni, Laetitia; Hauser, Daniel; Rothen-Rutishauser, Barbara; Zobi, Fabio. Recommanded Product: Bromopentacarbonylmanganese(I) And the article was included in Journal of Inorganic Biochemistry in 2020. The article conveys some information:

A series of tricarbonyl manganese complexes bearing 4-ethynyl-2,2′-bipyridine and 5-ethynyl-1,10-phenanthroline α-diimine ligands were synthesized, characterized and conjugated to vitamin B12, previously used as a vector for drug delivery, to take advantage of its water solubility and specificity toward cancer cells. The compounds act as photoactivatable carbon monoxide-releasing mols. rapidly liberating on average ca. 2.3 equiv of CO upon photo-irradiation Complexes and conjugates were tested for their anticancer effects, both in the dark and following photo-activation, against breast cancer MCF-7, lung carcinoma A549 and colon adenocarcinoma HT29 cell lines as well as immortalized human bronchial epithelial cells 16HBE14o- as the non-carcinogenic control. Our results indicate that the light-induced cytotoxicity these mols. can be attributed to both their released CO and to their CO-depleted metal fragments including liberated ligands. In the experiment, the researchers used many compounds, for example, Bromopentacarbonylmanganese(I)(cas: 14516-54-2Recommanded Product: Bromopentacarbonylmanganese(I))

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Recommanded Product: Bromopentacarbonylmanganese(I)

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《Metal-Templated, Tight Loop Conformation of a Cys-X-Cys Biomimetic Assembles a Dimanganese Complex》 was written by Le, Trung; Nguyen, Hao; Perez, Lisa M.; Darensbourg, Donald J.; Darensbourg, Marcetta Y.. Computed Properties of C5BrMnO5 And the article was included in Angewandte Chemie, International Edition in 2020. The article conveys some information:

With the goal of generating anionic analogs to MN2S2·Mn(CO)3Br the authors introduced metallodithiolate ligands, MN2S22- prepared from the Cys-X-Cys biomimetic, ema4- ligand (ema = N,N’-ethylenebis(mercaptoacetamide); M = NiII, [VIV O]2+ and FeIII) to Mn(CO)5Br. An unexpected, remarkably stable dimanganese product, (H2N2(CH2C:O(μ-S))2)[Mn(CO)3]2 resulted from loss of M originally residing in the N2S24- pocket, replaced by protonation at the amido nitrogens, generating H2ema2-. Accordingly, the ema ligand has switched its coordination mode from an N2S24- cavity holding a single metal, to a binucleating H2ema2- with bridging sulfurs and carboxamide oxygens within Mn-μ-S-CH2-C-O, 5-membered rings. In situ metal-templating by zinc ions gives quant. yields of the Mn2 product. By computational studies the authors compared the conformations of “”linear”” ema4- to ema4- frozen in the “”tight-loop”” around single metals, and to the “”looser”” fold possible for H2ema2- that is the optimal arrangement for binucleation. XRD mol. structures show extensive H-bonding at the amido-nitrogen protons in the solid state. In addition to this study using Bromopentacarbonylmanganese(I), there are many other studies that have used Bromopentacarbonylmanganese(I)(cas: 14516-54-2Computed Properties of C5BrMnO5) was used in this study.

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Computed Properties of C5BrMnO5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary