2-Ureido-1,3-thia­zol-3-ium dihydrogen phosphate

The title compound, C4H6N3OS+·H2PO4 −, (I), was obtained as a result of hydrolysis of [(1,3-thia­zol-2-yl­amino)­carbon­yl]­phospho­ramidic acid, (II), in water. X-ray analysis has shown that the N—P bond in (II) breaks, leading to the formation of the substituted carbamide (I). This compound exists as an inter­nal salt. The unit cell consists of a urea cation and an anion of H2PO4 −. Protonation of the N atom of the heterocyclic ring was confirmed by the location of the H atom in a difference Fourier map. The mol­ecules of substituted urea are connected by O⋯O hydrogen bonds into unlimited planes. In turn, those planes are connected to each other via N—H⋯O hydrogen bonds with mol­ecules of phospho­ric acid, forming a three-dimensional polymer

N-[Bis(benzylamino)phosphoryl]-2,2,2-trichloroacetamide

In the title compound, C16H17Cl3N3O2P, the P atom has a slightly distorted tetra­hedral configuration. The conformations of the carbonyl and phosphoryl groups are anti to each other. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into infinite chains parallel to the b axis

Bis(N-{bis­[meth­yl(phen­yl)amino]phos­phor­yl}-2,2,2-trichloro­acetamide)di­nitrato­dioxidouranium(VI)

In the title compound, [UO2 L 2(NO3)2] {L = N-{bis­[meth­yl(phen­yl)amino]phosphor­yl}-2,2,2-trichloro­acetamide, C16H17Cl3N3O2P}, the UVI ions are eight-coordinated by axial oxido ligands and six equatorial O atoms from the phosphoryl and nitrate groups in a distorted hexa­gonal–bipyramidal geometry. There are disordered fragments in the two coordinating L ligands: the trichloro­methyl group is rotationally disordered between two orientations [occupancy ratio 0.567 (15):0.433 (15)] in one ligand, and a meth­yl(phen­yl)amine fragment is disordered over two conformations [occupancy ratio 0.60 (4):0.40 (4)] in the other ligand. In the crystal structure, intra­molecular N—H⋯O hydrogen bonds between the amine and nitrate groups are observed

Bis{N-[bis­(pyrrolidin-1-yl)phosphor­yl]-2,2,2-trichloro­acetamide}di­nitrato­dioxidouranium(VI)

The crystal structure of the title compound, [U(NO3)2O2(C10H17Cl3N3O2P)2], is composed of centrosymmetric [UO2(L)2(NO3)2] mol­ecules {L is N-[bis­(pyrrolidin-1-yl)phosphor­yl]-2,2,2-trichloro­acetamide, C10H17Cl3N3O2P}. The UVI ion, located on an inversion center, is eight-coordinated with axial oxido ligands and six equatorial oxygen atoms of the phosphoryl and nitrate groups in a slightly distorted hexa­gonal-bipyramidal geometry. One of the pyrrolidine fragments in the ligand is disordered over two conformation (occupancy ratio 0.58:0.42). Intra­molecular N—H⋯O hydrogen bonds between the amine and nitrate groups are found

catena-Poly[neodymium(III)-bis­[μ-N-(dimorpholinophosphor­yl)benzene­sulfonamidato]-sodium(I)-bis­[μ-N-(dimorpholinophosphor­yl)benzene­sulfonamidato]]

The cubic crystal structure of the title compound, [NaNd(C14H21N3O5PS)4]n, is composed of one-dimensional polymeric chains propagating in [100], built up from [Nd(C14H21N3O5PS)4]− anions and sodium cations functioning as linkers. In the complex anion, the Nd3+ ion has an eightfold coordination environment formed by the sulfonyl and phosphoryl O atoms of four bidentate chelating N-(dimorpholinophosphor­yl)benzene­sulfonamidate ligands: the resulting NdO8 polyhedron can be described as inter­mediate between dodeca­hedral and square anti­prismatic. The sodium ion adopts an NaO4 tetra­hedral geometry arising from four monodentate benzene­sulfonamidate ligands. The resulting crystal structure is unusual because it contains substantial voids (800 Å3 per unit cell), within which there is no evidence of included solvent

Lanthanide Coordination Compounds with Monodentate Coordinated Β-diketone Heteroanalogue - (2,2,2-trichloro-n-(Dipiperidin-1-yl-phosphoryl)acetamide: Synthesis and Spectral Investigations

New mononuclear six-coordinate lanthanide coordination compounds [Ln (HL)3Cl3] (HL = (2,2,2-trichloro-N-(dipiperidin-1-yl-phosphoryl)acetamideCCl3C(O)N(H)P(O)[N(CH2)5]2, carbacylamidophosphate (CAPh) type ligand) have been synthesized from non-aqueous solutions. The complexes have been characterized by elemental analysis, spectroscopic methods (FTIR, 1H- and 31P-NMR, UV-Vis). The structure of [Sm(HL)3Cl3] has been further confirmed by single crystal X-ray diffraction analysis

catena-Poly[sodium-di-μ-aqua-sodium-bis[μ-2,2,2-trichloro-N-(dimorpholinophosphoryl)acetamide]]

The title compound, [Na2(C10H16Cl3N3O4P)2(H2O)2]n, can be considered as a two-dimensional coordination polymer in which one-dimensional chains are connected to each other by inter­molecular C—H⋯O hydrogen bonds involving the water mol­ecules. The NaI ion is five-coordinated in a distorted trigonal-bipyramidal geometry. The connection between the two NaI ions is facilitated by the two μ-O atoms of the carbonyl group of the 2,2,2-trichloro-N-(dimorpholino­phosphor­yl)acetamide (CAPh) ligand. A bridging coordination of the CAPh ligand via the carbonyl O atom is observed for the first time. The bridging water mol­ecules form inter­molecular O—H⋯O hydrogen bonds with the O atoms of the morpholine rings and the phosphoryl groups of neighboring CAPh mol­ecules

How minor structural changes generate major consequences in photophysical properties of RE coordination compounds; resonance effect, LMCT state

Lanthanide coordination compounds of the formula Na[Ln(L)4] (1Ln), where Ln ¼ La3þ, Eu3þ, Gd3þ, Tb3þ, L ¼ [L] and HL ¼ dimethyl(4-methylphenylsulfonyl)amidophosphate, were synthesized. Their structural and spectroscopic properties were discussed in detail based on X-ray diffraction measurements, IR spectroscopy, absorption and emission spectroscopy at 293 and 77 K and theoretical calculations of the intramolecular energy transfer (IET) rates. DFT calculations were used to investigate the 1Ln electronic properties required to calculate the transition rates. 30 and 22 pathways of intramolecular nonradiative energy transfer were examined in the case of 1Eu and 1Tb, respectively. It is shown that the main pathway for sensitization of the lanthanide emission is either the triplet (1Eu) or singlet (1Tb) transfer, occurring mainly through the exchange mechanism. The energy rates for energy transfer from S1 and T1 equal WS ¼ 1:53 105 s 1 (1Eu), WT ¼ 5:14 106 s 1 (1Eu) and WS ¼ 4:09 107 s 1 (1Tb), WT ¼ 6:88 105 s 1 (1Tb). The crucial role of the 7F5 level in the energy transfer process of 1Tb and the participation of the LMCTstate in the depopulation of the ligand singlet state of 1Eu were demonstrated. The influence of the resonance effect on the splitting of the 7F1 level in 1Eu was analyzed. By comparing the properties of 1Ln with the properties of 2Ln coordination compounds, sharing the same ligand and crystallizing in the same crystallographic system (monoclinic), but with a different space group, it is demonstrated how slight structural changes can affect the photophysical properties of Ln compounds.publishe

Improving the operational reliability of membranes and bellows with fluorinated surfactants

One of the characteristic properties of organofluorine compounds is their low surface energy. In this regard, surfactants containing perfluoroalkyl groups, as a rule, are much more effective than their nonfluorinated analogues. The unique character of fluorinated surfactants is also determined by their pronounced oleophobic properties. Surfaces treated with fluorinated surfactants are not only water-repellent, as in the case of their hydrocarbon analogues, but also benzo- and oil-repellent. Fluorotensides are highly resistant to oxidants and aggressive substances (acids, alkalis, chlorine, etc.). They also have high temperature resistance, withstand oxygen shock, have a solidification temperature of up to -160 °C, do not change properties at a dose rate of up to 108 rad. The applications of surfactants are extremely diverse. One of the methods of increasing the wear resistance of friction pairs is the method of surface treatment of friction pairs with fluorotensides. Fluorotensides are multicomponent systems that include organofluorine surfactants in various solvents and regulatory additives. In Russia, brands of fluorotensides have been created that surpass foreign samples in many respects, which has significantly expanded the scope of their application

Luminescent Thin Films Based on N-(Diphenylphosphoryl)benzamide EuIII and TbIII Complexes for Light Emitting Diode Technology

The lanthanides coordination compounds LnL3, LnL3Phen and LnL3Dipy with bulky aryl-functionalised carbacylamidophosphate (CAPh) ligand N-(diphenylphosphoryl)benzamide (HL=PhC(O)N(H)P(O)Ph2) were synthesized for luminescent thin films producing. The films were obtained by vacuum evaporation and spin coating methods and exhibited intensive monochromatic photoemission with decay times equal to 0.78 1.34 ms