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The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: cis-Dichlorobis(pyridine)platinum(II)(SMILESS: [Cl-][Pt+2]([N]1=CC=CC=C1)([Cl-])[N]2=CC=CC=C2,cas:15227-42-6) is researched.Recommanded Product: 92-71-7. The article 《Pyrrole thioaldehyde complexes of nickel, palladium and platinum》 in relation to this compound, is published in Zeitschrift fuer Naturforschung, B: Chemical Sciences. Let’s take a look at the latest research on this compound (cas:15227-42-6).

The coordination chem. of the unusual, pyrrole-stabilized thioaldehyde mols., 3,5-dimethylpyrrole-2-carbothioaldehyde (HSPyMeHMe) and 3,5-dimethyl-4-ethylpyrrole-2-carbothioaldehyde (HSPyMeEtMe) was studied with nickel, palladium and platinum in preparing [M(κ2-SPyMeRMe)2] (M = Ni, Pd, Pt; R = H, Et). The structure of the cyclometalated derivative [Pd(η2-C,N-C6H4CH2-2-NMe2)(κ2-SPyMeEtME)] was determined by x-ray diffraction.

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SDS of cas: 1452-77-3. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: Picolinamide, is researched, Molecular C6H6N2O, CAS is 1452-77-3, about Bis-heteroleptic ruthenium(II) complex with 2-picolinamide: Synthesis, crystal structures, and spectroscopic study for anion recognition using the amide group. Author is Toyama, Mari; Fujii, Yudai; Endo, Mika.

Cis-[Ru(bpy)2(OH2)2](OTf)2 (1·(OTf)2; OTf- = CF3SO3-) was reacted with 2-picolinamide (H2pia) in EtOH to form bis-heteroleptic complex [Ru(bpy)2(H2pia)]X2 (2·X2; X- = OTf- or Cl-). Crystal structures of 2·X2 revealed that H2pia was coordinated to Ru(II) through N of pyridyl group and O of amide group to form the N,O-coordination, and acted as a neutral ligand. Bond distances around the amide group and 1H NMR study for 22+ suggested that π-electron on the carbonyl group was delocalized to the whole amide group. Adding F- to the acetonitrile solution of 2·(OTf)2 changed the red solution to dark-red due to the transportation of π-electron on the amide group by the bound F- to the amide H. Absorption and 1H NMR spectroscopies revealed that the NH2 of 22+ undergoes selective two-step adduct reaction with F-: the H close to pyridyl group of H2pia first formed a 1:1 adduct (mono-F-adduct-22+), followed by the other H forming the 1:2 adduct (di-F-adduct-22+). Adding excess Li(OTf) to these F-adduct-22+ solutions changed the dark-red solution back to red, suggesting that the adducted F- was removed by Li+ to form 22+ and LiF.

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Recommanded Product: 1-Bromoundecane. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 1-Bromoundecane, is researched, Molecular C11H23Br, CAS is 693-67-4, about Amphiphilic Star-Shaped Calix[4]resorcinarene as Stationary Phase for Capillary Gas Chromatography. Author is Sun, Tao; Li, Bin; Li, Yan; Zhao, Xinyu; Song, Qianqian; Jiang, Xingxing; Shuai, Xiaomin; Li, Youyang; Cai, Zhiqiang; Hu, Shaoqiang.

This work describes the separation performance of the amphiphilic star-shaped calix[4]resorcinarene (C4A-CL)(I) as the stationary phase for capillary gas chromatog. (GC). The statically coated C4A-CL capillary column exhibited medium polarity and high column efficiency of 3877 plates m-1 determined by naphthalene at 120 °C. Importantly, the C4A-CL column exhibited extremely high resolving capability for aliphatic analytes with varying polarity, including n-alkanes, esters, ketones, alcs., and bromoalkanes. In addition, the C4A-CL column exhibited high selectivity and resolving capability for positional, structural and cis-/trans-isomers. Among them, the C4A-CL column displayed advantageous resolving capability over the com. DB-17 column for aromatic amine isomers. Moreover, it was applied for the determination of isomer impurities in real samples, showing good potential in GC applications.

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In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Synthesis and biological evaluation of novel bis-quaternary ammonium compounds with p-terphenyl spacer, published in 2020-07-31, which mentions a compound: 693-67-4, Name is 1-Bromoundecane, Molecular C11H23Br, Formula: C11H23Br.

Bis-quaternary ammonium compounds I·2 Br- [R = H(CH2)n; n = 7, 8, 9, 10, 11] with a p-terphenyl spacer between two pyridinium heads were synthesized. I·2 Br- (n = 8) was superior to the known benzalkonium chloride, miramistin and chlorhexidine bisgluconate in its MIC values against five pathogenic bacteria.

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Let`s talk about compounds: 15227-42-6

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Recommanded Product: cis-Dichlorobis(pyridine)platinum(II). The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: cis-Dichlorobis(pyridine)platinum(II), is researched, Molecular C10H10Cl2N2Pt, CAS is 15227-42-6, about Stereospecific synthesis of cyclobutanol derivatives using a 5 minus 1 methodology and platinum(II). Author is Stewart, Frederick F.; Jennings, P. W..

Cycloaddition reaction of the carbene N2CHCO2Et to norbornene in the presence of Rh(II) gave 95% tricyclic esters I (R = CO2Et), which were reduced with LiAlH4 to give 63% I (R = CH2OH) (II). Kinetic resolution of II by oxidative insertion with Pt(py)2Cl2 gave 93% complex III (R = CH2OH) and its isomer, which underwent stereospecific acid-catalyzed ring expansion to give 70-80% complexes IV (R1 = H, Me, CHO; L = py) and their isomers. Ligand substitution with P(OMe)3 gave 100% IV [L = P(OMe)3], which underwent reductive elimination on heating to give 80-90% III (R = OR1).

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The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Crystal and molecular structures of cis- and trans-dichlorobis(pyridine)platinum(II)》. Authors are Colamarino, Paolo; Orioli, Pier L..The article about the compound:cis-Dichlorobis(pyridine)platinum(II)cas:15227-42-6,SMILESS:[Cl-][Pt+2]([N]1=CC=CC=C1)([Cl-])[N]2=CC=CC=C2).SDS of cas: 15227-42-6. Through the article, more information about this compound (cas:15227-42-6) is conveyed.

The crystal and mol. structures of cis- and trans-dichlorobis(pyridine)platinum (I, II resp.) were determined from x-ray diffractometer data by heavy-atom techniques and refined by least squares to R 0.041 and 0.068 for 1000 and 1032 observed intensities for I and II, resp. Crystals of I are monoclinic, space group C2/c, with a 9.408, b 17.110, c 15.270 Å, β 98.53.degree., and Z = 8. Crystals of II are triclinic, space group P1̅, with a 7.695, b 7.091, c 5.542 Å, α 87.6, β 83.7, γ 79.3.degree., and Z = 1. Both complexes consist of discrete mols. with Pt in square planar coordination.

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Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: cis-Dichlorobis(pyridine)platinum(II), is researched, Molecular C10H10Cl2N2Pt, CAS is 15227-42-6, about Mass spectrometry of platinum(II) complexes. Comparison of cis and trans isomers. Fragmentation and rearrangement pathways.Synthetic Route of C10H10Cl2N2Pt.

The mass spectra of 8 pairs of cis and trans isomers of PtL2X2 (L=NH3, pyridine PEt3, or PPh3; X=Cl, Br, or I) are presented and discussed. Two chelates, Pt(bipy)Cl2 and Pt(dpm)Cl2(dpm=di-α-pyridylmethane), are also included. The most significant results are: (1) parent ions can be observed for almost all these relatively involatile coordination compounds; (2) most ligand fragmentations and rearrangements occur with ligand-metal bonds intact; (3) some rearrangements appear to involve the metal; (4) cis and trans isomers of phosphine complexes give different fragmentation patterns; (5) spectra of chelates differ considerably from the spectra of analogous nonchelates; (6) in Pt(NH3)2Cl2 and Pt(py)2Cl2, little or no difference is observed in the spectra of cis and trans isomers after electron impact. Therefore, excitation to a tetrahedral state may take place.

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Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 15227-42-6, is researched, Molecular C10H10Cl2N2Pt, about Far infrared spectra of palladium compounds. II. Pyridine and 2,2′-bipyridyl complexes of palladium(II) and platinum(II), the main research direction is PALLADIUM COMPLEX IR SPECTRA; IR SPECTRA PD COMPLEX; PLATINUM COMPLEX; PYRIDINE COMPLEX; BIPYRIDYL COMPLEX.Application In Synthesis of cis-Dichlorobis(pyridine)platinum(II).

The IR spectra of several sq. planar cis and trans Pd(II) and Pt(II) pyridine complexes of the type M(py)2X2 (where X = Cl, Br, and I) have been recorded from 2000 to 50 cm.-1 Comparison of the spectra of complexed pyridine to that of the free base shows 9 normal vibrations have shifted to higher frequencies on the order of 15 to 80 wave numbers The shifts are attributed to changes in the electron d. over the pyridine ring. Only insignificant shifts in a few of the normal modes of the complexed pyridine were observed between the corresponding cis and trans isomers. The assignment of the M-X stretching and bending vibrations as well as possible assignments for the M-N stretching vibrations are given and discussed. The IR spectra of Pd(II)-2,2-bipyridyl (bipy) complexes of the type Pd(bipy)2X2 (where X = Cl, Br, and I) were also recorded from 2000 to 50 cm.-1 Comparison of the spectra to those of the pyridine complexes and the free bipyridine is made. 18 references.

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Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 15227-42-6, is researched, Molecular C10H10Cl2N2Pt, about Cis-bis(pyridine)dichloro derivatives of platinum(IV), the main research direction is pyridine chloride complex Pt; chloride pyridine complex Pt; platinum pyridine chloride complex.Electric Literature of C10H10Cl2N2Pt.

The complexes Pt(py)2Cl2XNO2 (X = Cl-, Br-) and Pt(py)2Cl2(OH)NO2 were precipitated by adding 5-10 ml. H2O to mixtures of equivalent amounts of Pt(py)2Cl2(NO2)NO3 (I) and KCl, KBr, or KOH, resp. I reacts with KI to give a mixture of Pt(py)2Cl2I2 and Pt(py)2Cl2INO2. Chlorination of Pt(py)2Cl2 yields [Pt(py)2Cl2]Cl2. [Pt(py)2Cl2][Pt(py)2Cl2(OH)2] was obtained from Pt(py)2Cl2 and 10% aqueous H2O2 at room temperature after standing for 24 hrs. Individual species were identified by x-ray diffraction tests. The aqueous solutions of Pt(py)2Cl2XNO2 undergo hydrolysis according to: Pt(py)2Cl2XNO2 + H2O ⇌ [Pt(py)2Cl2X(H2O)]+ + NO2-, whereas the aqueous solutions of Pt(py)2Cl2(OH)2 and [Pt(py)2Cl2]Cl2 are considerably more stable. Solutions of Pt(py)2Cl2Br2 partially decompose in light to Pt(py)2Cl2, HBrO, and HBr, resp.

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Canty, Allan J.; Stevens, Elizabeth A. published the article 《Synthesis of potential platinum(II) antitumor complexes: complexes containing bidentate pyridyl and imidazolyl donors》. Keywords: antitumor platinum dipyridylmethane pyridylimidazole complex; imidazole pyridyl platinum antitumor complex.They researched the compound: cis-Dichlorobis(pyridine)platinum(II)( cas:15227-42-6 ).Recommanded Product: 15227-42-6. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:15227-42-6) here.

PtLCl2 [L = di-2-pyridylmethane, 3,3-bis(2-pyridyl)pentane, 2-(2-pyridyl)imidazole (I), N-methyl-2-(2-pyridyl)imidazole] were prepared and characterized by chem. anal., elec. conductivity, IR spectra, and inhibitory effects on cultures of L1210 mouse leukemia cells. The complex with L = I gave a 50% inhibiting dose similar to that of cis-Pt(NH3)2Cl2 and below the values of the other complexes; this suggests that further tests with tumor-bearing animals is warranted for this I complex with Pt.

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