Terminal Coordination Research Articles

Semantic segmentation-based detection algorithm for challenging cryo-electron microscopy RNP samples.

In this study, we present a novel and robust methodology for the automatic detection of influenza A virus ribonucleoproteins (RNPs) in single-particle cryo-electron microscopy (cryo-EM) images. Utilizing a U-net architecture-a type of convolutional neural network renowned for its efficiency in biomedical image segmentation-our approach is based on a pretraining phase with a dataset annotated through visual inspection. This dataset facilitates the precise identification of filamentous RNPs, including the localization of the filaments and their terminal coordinates. A key feature of our method is the application of semantic segmentation techniques, enabling the automated categorization of micrograph pixels into distinct classifications of particle and background. This deep learning strategy allows to robustly detect these intricate particles, a crucial step in achieving high-resolution reconstructions in cryo-EM studies. To encourage collaborative advancements in the field, we have made our routines, the pretrained U-net model, and the training dataset publicly accessible. The reproducibility and accessibility of these resources aim to facilitate further research and validation in the realm of cryo-EM image analysis.

On human nanoscale synaptome: Morphology modeling and storage estimation.

One of the key challenges in neuroscience is to generate the human nanoscale connectome which requires comprehensive knowledge of synaptome forming the neural microcircuits. The synaptic architecture determines limits of individual mental capacity and provides the framework for understanding neurologic disorders. Here, I address morphology modeling and storage estimation for the human synaptome at the nanoscale. A synapse is defined as a pair of pairs [(presynaptic_neuron),(presynaptic_axonal_terminal);(postsynaptic_neuron),(postsynaptic_dendritic_terminal)]. Center coordinates, radius, and identifier characterize a dendritic or axonal terminal. A synapse comprises topology with the paired neuron and terminal identifiers, location with terminal coordinates, and geometry with terminal radii. The storage required for the synaptome depends on the number of synapses and storage necessary for a single synapse determined by a synaptic model. I introduce three synaptic models: topologic with topology, point with topology and location, and geometric with topology, location, and geometry. To accommodate for a wide range of variations in the numbers of neurons and synapses reported in the literature, four cases of neurons (30;86;100;138 billion) and three cases of synapses per neuron (1,000;10,000;30,000) are considered with three full and simplified (to reduce storage) synaptic models resulting in total 72 cases of storage estimation. The full(simplified) synaptic model of the entire human brain requires from 0.21(0.14) petabytes (PB) to 28.98(18.63) PB for the topologic model, from 0.57(0.32) PB to 78.66(43.47) PB for the point model, and from 0.69(0.38) PB to 95.22(51.75) PB for the geometric model. The full(simplified) synaptic model of the cortex needs from 86.80(55.80) TB to 2.60(1.67) PB for the topologic model, from 235.60(130.02) TB to 7.07(3.91) PB for the point model, and from 285.20(155.00) TB to 8.56(4.65) PB for the geometric model. The topologic model is sufficient to compute the connectome's topology, but it is still too big to be stored on today's top supercomputers related to neuroscience. Frontier, the world's most powerful supercomputer for 86 billion neurons can handle the nanoscale synaptome in the range of 1,000-10,000 synapses per neuron. To my best knowledge, this is the first big data work attempting to provide storage estimation for the human nanoscale synaptome.

ANALISIS PEMBERLAKUAN TARIF MIKRO ANGKUTAN ANTAR KOTA TRAYEK KOTA GORONTALO PAGUAT

Analysis of the Implementation of Micro Tariffs for Inter-City Transport on the Gorontalo Paguat City Route. The aim of this research was to overcome the existence of micro drivers who charge their own transportation rates which are not in accordance with the provisions of established regulations. With the data collection method, interviews or in the context of this research, they are called informants. In this data source, the informants include the drivers, the Head of the Talaga Terminal Coordinator, Gorotalo City and the community, place, namely the data source obtained from a description of the situation and conditions related to the problem being discussed, Paper, namely the data source that presents signs in the form of letters. , numbers, images, or symbols. Based on the district regulation. Gorontalo number 28 of 2013 concerning adjustments to passenger transportation rates between cities, sub-districts and rural areas for economy class, namely Rp. 437.46,- /km/pnp. Based on these regulations, the Gorontalo-Paguat route is approximately 145km, namely Rp. 63,431,- or around Rp. 63,500,-. Meanwhile, the fare applied by micro drivers is Rp. 75,000. This is due to the large deposits made to the PO which covers the drivers, as well as the increasingly high cost of living necessities, therefore the government needs to review the determination of micro tariffs for public transport on the Gorontalo-Paguat route.

Synthesis, crystal structure and thermal decomposition pathway of bis-(iso-seleno-cyanato-κN)tetra-kis-(pyridine-κN)manganese(II).

The reaction of MnCl2·2H2O with KSeCN and pyridine in water leads to the formation of the title complex, [Mn(NCSe)2(C5H5N)4], which is isotypic to its Fe, Co, Ni, Zn and Cd analogues. In its crystal structure, discrete complexes are observed that are located on centres of inversion. The Mn cations are octa-hedrally coordinated by four pyridine coligands and two seleno-cyanate anions that coordinate via the N atom to the metal centres to generate trans-MnN(s)2N(p)4 octa-hedra (s= seleno-cyanate and p= pyridine). In the extended structure, weak C-H⋯Se contacts are observed. Powder X-ray diffraction (PXRD) investigations prove that a pure sample was obtained and in the IR and Raman spectra, the C-N stretching vibrations are observed at 2058 and 2060 cm-1, respectively, in agreement with the terminal coordination of the seleno-cyanate anions. Thermogravimetric investigations reveal that the pyridine coligands are removed in two separate steps. In the first mass loss, a compound with the composition Mn(NCSe)2(C5H5N)2 is formed, whereas in the second mass loss, the remaining pyridine ligands are removed, which is superimposed with the decomposition of Mn(NCSe)2 formed after ligand removal. In the inter-mediate compound Mn(NCSe)2(C5H5N)2, the CN stretching vibration is observed at 2090 cm-1 in the Raman and at 2099 cm-1 in the IR spectra, indicating that the Mn cations are linked by μ-1,3-bridging anionic ligands. PXRD measurements show that a compound has formed that is of poor crystallinity. A comparison of the powder pattern with that calculated for the previously reported Cd(NCSe)2(C5H5N)2 indicates that these compounds are isotypic, which was proven by a Pawley fit.

Magnetic properties and pH-controlled reversible interconversion of µ-oxido into µ-hydroxido in oxo-carboxylato bridged iron(III) dimers: Theoretical and experimental insights

Three dinuclear complexes of formula [FeIII2(µ-O)(µ-OOCR)(L)2](ClO4)·G, with R/G=H/(EtOAc)2 (1·2EtOAc), CH3/(Et2O)2 (2·2Et2O) and C6H5/(CH3OH)2(CH3CN)2 (3·2CH3OH·2CH3CN), [where HL = 2-((((1-methylbenzimidazol-2-yl)methyl)(pyridin-2-ylmethyl)amino)methyl)phenol] have been prepared. The ligand provides a N,N,N,O donor set in its deprotonated form. X-ray diffraction analyses revealed that the complexes have a similar oxido-carboxylato-bridged structure where each metal ion has a tertiary amine, one imidazolyl N atom, one pyridyl N atom and a phenolate O atom as terminal coordination. Thus, each metal centre assumes a FeIIIN3O3 coordination in an octahedral environment. Addition of acid lead to the generation of similar dinuclear complexes formulated as [FeIII2(µ-OH)(µ-OOCR)(L)2](ClO4)2, with R=H (1H), CH3 (2H) and C6H5 (3H) in solution. This protonation of the µ-O bridge is reversible and addition of base regenerates the original complexes (1–3). Magnetic measurements showed intramolecular antiferromagnetic Fe···Fe interactions in compounds 1–3 with J = ‒276(1), ‒197(1) and ‒190(1) cm−1, respectively. DFT/B3LYP calculation helped us to explicitly state the sign and magnitude of the magnetic coupling constants along with an approaching to the spin density distribution.

Chiral All-Nitrogen-Coordinated Dysprosium Single-Molecule Magnets.

Two pairs of chiral end-on azido-bridged dinuclear hexaazamacrocycles, [Dy2 (LN6 R/S )2 (N3 )2 Cl2 ](BPh4 )2 (1R/1S) and [Dy2 (LN6 R/S )2 (N3 )4 ]Cl2 (2R/2S) (LN6 R/S is hexaazamacrocyclic neutral Schiff base ligand derived from 2,6-diformylpyridine and (1R, 2R)/(1S, 2S)-diaminocyclohexane), were constructed by adjusting the molar ratio of sodium azide to Dy(III) macrocycle precursor. Structural analyses reveal that all Dy(III) centers in complexes 1R/1S and 2R/2S are nine-coordinate with hula-loop coordination geometry, and the differences between 1R/1S and 2R/2S are the terminal coordination anion and counter anion. Magnetic studies indicate that complex 2S displays typical SMM behaviors under a zero dc field, whereas 1S just shows slow relaxation of magnetization resulting from a relatively weak axial crystal field. Significantly, complex 2R/2S represents the first homochiral all-nitrogen-coordinated lanthanide single-molecule magnet.

Synthesis and Characterization of Lanthanide Metal Ion Complexes of New Polydentate Hydrazone Schiff Base Ligand

The new homodinuclear complexes of the general formula [Ln2L3(NO3)3] (where HL is newly synthesized 2-((2-(benzoxazol-2-yl)-2-methylhydrazono)methyl)phenol and Ln = Sm3+ (1), Eu3+ (2), Tb3+ (3a, 3b), Dy3+ (4), Ho3+ (5), Er3+ (6), Tm3+ (7), Yb3+ (8)), have been synthesized from the lanthanide(III) nitrates with the polydentate hydrazone Schiff base ligand. The flexibility of this unsymmetrical Schiff base ligand containing N2O binding moiety, attractive for lanthanide metal ions, allowed for a self-assembly of these complexes. The compounds were characterized by spectroscopic data (ESI-MS, IR, UV/Vis, luminescence) and by the X-ray structure determination of the single crystals, all of which appeared to be different solvents. The analytical data suggested 2:3 metal:ligand stoichiometry in these complexes, and this was further confirmed by the structural results. The metal cations are nine-coordinated, by nitrogen and oxygen donor atoms. The complexes are two-centered, with three oxygen atoms in bridging positions. There are two types of structures, differing by the sources of terminal (non-bridging) coordination centers (group A: two ligands, one nitro anion/one ligand, two nitro anions, group B: three ligands, three anions).

Chemistry of a Nitrosyl Ligand κ:η-Bridging a Ditungsten Center: Rearrangement and N-O Bond Cleavage Reactions.

The novel nitrosyl-bridged complex [W2Cp2(μ-PtBu2)(μ-κ:η-NO)(CO)(NO)](BAr4) [Ar = 3,5-C6H3(CF3)2] was prepared in a multistep procedure starting from the hydride [W2Cp2(μ-H)(μ-PtBu2)(CO)4] and involving the new complexes [W2Cp2(μ-PtBu2)(CO)4](BF4), [W2Cp2(μ-PtBu2)(CO)2(NO)2](BAr4), and [W2(μ-κ:η5-C5H4)Cp(μ-PtBu2)(CO)(NO)2] as intermediates, which follow from reactions with HBF4·OEt2, NO, and Me3NO·2H2O, respectively. The nitrosyl-bridged cation easily added chloride upon reaction with [N(PPh3)2]Cl, with concomitant NO rearrangement into the terminal coordination mode, to give [W2ClCp2(μ-PtBu2)(CO)(NO)2], and underwent N–O and W–W bond cleavages upon the addition of CNtBu to give the mononuclear phosphinoimido complex [WCp(NPtBu2)(CNtBu)2](BAr4). Another N–O bond cleavage was induced upon photochemical decarbonylation at 243 K, which gave the oxo- and phosphinito-bridged nitrido complex [W2Cp2(N)(μ-O)(μ-OPtBu2)(NO)](BAr4), likely resulting from a N–O bond cleavage step following decarbonylation.

Artificial Intelligence Monitoring System Using ZigBee Wireless Network Technology in Warehousing and Logistics Innovation and Economic Cost Management

The study expects to reduce the development cost and energy consumption of the storage environment monitoring and improve the efficiency of the storage monitoring environment. Firstly, the storage environment monitoring system is designed in detail using ZigBee. It includes the design of terminal nodes, router nodes, coordinator nodes, and upper computer software. Here is a detailed description of the process of establishing a communication network for three different types of devices in the ZigBee network. The address allocation mechanism of the ZigBee network is introduced. Then, through the application of activity-based costing, the cost reduction is achieved as expected. Finally, the evaluation model of the storage logistics cost level is established, and the various reasons that affect the storage logistics cost are analyzed. The completed warehouse environment monitoring system is a tree topology network composed of a ZigBee coordinator, several ZigBee routing nodes, and terminal devices through the above design. The coordinator in the network is responsible for establishing the network, and it can communicate with the host computer through the serial port. The terminal node collects environmental parameter information and feeds the data back to the ZigBee coordinator through wireless multihop. The ZigBee routing node is mainly used to expand the range of the network to achieve the purpose of wireless monitoring of the entire storage environment. This provides a reference for the combination of wireless communication technology and sensor technology.

A facile method to enhance the output performance of triboelectric nanogenerators based on coordination polymers by modulating terminal coordination groups

Three isostructural Cu(i)-CPs with different terminal halogen atoms were introduced into the fabrication of TENGs, and were further applied for self-powered electrochemical cathodic protection.

Homochiral Ferromagnetic Coupling Dy2 Single-Molecule Magnets with Strong Magneto-Optical Faraday Effects at Room Temperature.

By the bridging action of the 6-chloro-2-hydroxypyridine (Hchp) ligand and the terminal coordination role of the homochiral ligand, (-)/(+)-3-trifluoroacetyl camphor (l-Htfc/d-Htfc), a pair of enantiomerically pure dysprosium(III) dinuclear complexes, [Dy2(l-tfc)4(chp)2(MeOH)2] (l-1) and [Dy2(d-tfc)4(chp)2(MeOH)2] (d-1), was obtained. Their circular dichroism (CD) spectra verified their enantiomeric nature. Magnetic investigation indicated that they exhibit ferromagnetic interaction and good zero field single-molecule magnet (SMM) properties. The Ueff/k values of l-1 and d-1 at 0 Oe are 180.5 and 181.3 K, respectively, which are large values for homochiral Dy(III) SMMs. A reasonable explanation for the magnetic properties of l-1 and d-1 was supplied by ab initio calculations. Remarkably, magnetic circular dichroism (MCD) investigation revealed that the chiral Dy2 enantiomers show a strong magneto-optical Faraday effect at room temperature, suggesting potential applications in magneto-optical devices.

Copper(I) azide and copper(I) cyanate π-complexes

Electrochemical alternating current synthesis starting from an ethanol solution of CuSO4 · 5H2O and allylamine in the presence of solid sodium azide results in formation of Cu[C3H5NH2]N3. The trigonal-pyramidal coordination environment of both crystallographically independent copper ions consists of the C = C-bond of one allylamine molecule, the NH2-group of another ligand moiety and two N-atoms of the two azide-anions. One N3 − exhibits a terminal coordination mode and the other is a μ3-1,1,3-bridge. The bridging function of both allylamine and azide leads to formation of a complicated 3-D network. An elongation of coordinated C = C-bond and a strong shift of the ν s mode in the Raman spectrum confirm effective Cu–(C = C) bonding. A similar synthetic route starting from a methanol solution of Cu(BF4)2 · 6H2O in the presence of solid potassium cyanate results in formation of Cu[C3H5NH2]NCO. The cyanate-anion is bound to copper through nitrogen. The nitrogen from the allylamine molecule and the C = C-bond from another ligand complete the trigonal-planar environment of copper. The elongation of the coordinated C = C-bond and the shift of ν s (C = C) mode in the Raman spectrum are similar to those in the azide derivative.

Synthesis, X-ray structure, Hirshfeld analysis and DFT studies of Ni(II) complexes with pyridine-type ligands and monoanionic (SCN¯, N3¯ and NO3¯) ligands

The molecular and supramolecular structures of two self-assembled Ni(II) complexes with pyridine-type ligands (34Lut: 3,4-lutidine and 4Pic: 4-picoline) comprising different anions (SCN¯, N3¯and NO3¯) were presented. The dinuclear [Ni(34Lut)3(SCN)2]2(1) complexcomprises a hexa-coordinated Ni(II) with NiN5S coordination environment from three 34Lut, one isothiocyanate, in addition to two SCN¯ connecting the two Ni(II) centres via µ(1,3) coordination mode. Structure of complex 2 has the two complex units [Ni(4Pic)4(N3)2][Ni(4Pic)4(NO3)2], in which the two Ni(II) centers have also hexa-coordinated environments with NiN6 and NiN4O2 coordination spheres. In both units, there are four 4Pic ligand units coordinating the Ni(II) via the pyridine nitrogen atom and two anions in anti-positions to one another. In the first unit, the two azides have terminal coordination mode. In the second unit, there are two monodentate nitrate ions coordinating the Ni(II) ion via one oxygen atom. Molecular packing analysis using Hirshfeld calculations revealed the importance of the S…H (20.4%) and CH…π (25.2%) interactions in 1. For complex 2, the N…H (16.2%) and O…H (20.7%) contacts are the most important in [Ni(4Pic)4(N3)2] and [Ni(4Pic)4(NO3)2] complex units, respectively. The H…H contact percentages are 50.5, 54.6 and 51.3%, respectively which are the most common in all complex units. Using DFT calculations, the charge of the Ni(II) ion decreased to 0.7792, 0.8136 and 0.9377 e in the thiocyanato, azido and nitrato complexes, respectively. Using AIM calculations, the Ni-N, Ni-S and Ni-O bonds showed the characteristics of mainly closed shell interactions.

Synthesis, crystal structures and catalytic activity of oxidovanadium(V) complexes with tridentate ONO aroylhydrazone ligands

Two oxidovanadium(V) complexes, [VOL1(OEt)] (1) and [V2O2(L2)2(OEt)2] (2), where L1 and L2 are the anions of 2-amino-N′-(2-hydroxybenzylidene)benzohydrazide (H2L1) and N′-(2-hydroxybenzylidene)-4-hydroxybenzohydrazide (H2L2), respectively, have been synthesized and characterized by elemental analysis, infrared and electronic spectra, and 1H NMR spectra. Structures of the complexes were further confirmed by single-crystal X-ray determination. The V atom in the mononuclear complex 1 is in square pyramidal coordination, and those in the dinuclear complex 2 are in octahedral coordination. Both aroylhydrazone ligands coordinate to the V atoms through the phenolate O, imino N, and enolate O atoms. The ethanol ligand in complex 1 is in terminal coordination mode, while that in complex 2 is in bridging coordination mode. The complexes function as effective olefin epoxidation catalysts with hydrogen peroxide as terminal oxidant and sodium hydrogen carbonate as a co-catalyst.

Structure and State of Water in Branched N-Vinylpyrrolidone Copolymers as Carriers of a Hydrophilic Biologically Active Compound.

Hydrated copolymers of N-vinylpyrrolidone (VP) with triethylene glycol dimethacrylate as a promising platform for biologically active compounds (BAC) were investigated by different physical chemical methods (dynamic light scattering, infrared spectroscopy, thermal gravimetric analysis, and differential scanning calorimetry) and the quantum chemical modeling of water coordination by the copolymers in a solution. According to the quantum chemical simulation, one to two water molecules can coordinate on one O-atom of the lactam ring of VP units in the copolymer. Besides the usual terminal coordination, the water molecule can form bridges to bind two adjacent C=O groups of the lactam rings of VP units. In addition to the first hydration shell, the formation of a second one is also possible due to the chain addition of water molecules, and its structure depends on a mutual orientation of C=O groups. We showed that N,N-dimethylbiguanidine hydrochloride (metformin) as a frontline drug for the treatment of type 2 diabetes mellitus can be associated in aqueous solutions with free and hydrated C=O groups of the lactam rings of VP units in studied copolymers. Based on the characteristics of the H-bonds, we believe that the level of the copolymer hydration does not affect the behavior and biological activity of this drug, but the binding of metformin with the amphiphilic copolymer will delight in the penetration of a hydrophilic drug across a cell membrane to increase its bioavailability.

A Series of Manganese(III) Salen Complexes as a Result of Team-Based Inquiry in a Transnational Education Programme.

The development of a team-based approach to research-led transnational practical chemistry teaching is described in which a team of five Chinese students on an articulated transnational degree programme, supported by a team of academic and technical staff, carried out a study examining the structural chemistry of a series of manganese(III) salen complexes. A series of four crystallographically characterized manganese(III) salen complexes with ancillary carboxylate ligands are reported here. The carboxylate coordination modes range from the bridging syn-anti μ2 -κO : κO' mode observed in the predominant cyclohexanoate and isobutyrate species, to a capping terminal monodentate mode for the adamantanoate species, and an unusual mixture of bridging and terminal coordination modes observed in a second minor phase of the cyclohexanoate species. The variation on extended structures based on the weakly interacting aliphatic backbones may provide a useful basis for further structural studies.

Quantum Chemical Modeling the Structure of Complexes of Copolymer of N-Vinylpyrrolidone and Triethylene Glycol Dimethacrylate with Metformin

The structure of metformin (dimethylbiguanide) complexes with the copolymer of N-vinylpyrrolidone and triethylene glycol dimethacrylate in aqueous solutions is studied by means of DFT (Gaussian 09 software; TPSSh functional; 6-31G*//6-311++G** basis set) and the QTAIM model (AIMALL software). It is shown that both metformin and water molecules coordinate via the oxygen atom of the С=O bond of lactam rings, and that this process is exothermic. One oxygen atom can coordinate one or two water molecules, and water can form bridges connecting two adjacent C=O groups in addition to common terminal coordination. The formation of the second hydration shell after the formation of the first is possible due to the chain addition of water molecules; its structure depends on the mutual orientation of the С=О groups. It was shown that metformin is oriented with respect to electron donor groups in a strictly determined way; it can displace water upon coordination with the copolymer.

Terminal location method with NLOS exclusion based on unsupervised learning in 5G‐LEO satellite communication systems

SummaryWe investigate the terminal location method in 5G‐Low Earth Orbit (5G‐LEO) satellite communication systems. To overcome the dependence on the external Global Navigation Satellite System (GNSS), we propose to use a single LEO satellite in 5G‐LEO satellite communication systems for terminal location and utilize the downlink synchronization detection for pseudorange differential measurement. Then, a data clustering method of unsupervised machine learning is proposed to classify the measured data into line‐of‐sight (LOS) and non‐line‐of‐sight (NLOS) signals. Furthermore, the NLOS data are excluded, and the Taylor series expansion iteration method is used to calculate the terminal coordinates. Simulation results show that the proposed method can effectively reduce the influence of NLOS error on measurement results and improve the accuracy of terminal location. In simulated urban scenario, the average location accuracy is improved from 10 km by traditional methods to 0.7 km and the convergence time is reduced from 400 to 250s.

Palladium carbonyl complexes with anions of N-heterocyclic carboxylic and pyridine-2-sulfonic acids

Synthesis, spectral characteristics, and structure of palladium(I) carbonyl complexes containing anions of N-heterocyclic carboxylic acids and pyridine-2-sulfonic acid of the general formula [Pd(CO)(NHC-CO2)]n/[Pd(CO)(NHC-SO3)]n, where NHC is an N-heterocycle, were described. The resulting complexes can be attributed to a binuclear structure with bridging or terminal coordination of carbonyl ligands depending on the nature of the substituents in the heterocycle.

Chromium complexes bearing disubstituted organophosphate ligands and their use in ethylene polymerization.

The crystal structures of three unusual chromium organophosphate complexes have been determined, namely, bis(μ-butyl 2,6-di-tert-butyl-4-methylphenyl hydrogen phosphato-κO:κO')di-μ-hydroxido-bis[(butyl 2,6-di-tert-butyl-4-methylphenyl hydrogen phosphato-κO)(butyl 2,6-di-tert-butyl-4-methylphenyl phosphato-κO)chromium](Cr-Cr) heptane disolvate or {Cr2(μ2-OH)2[μ2-PO2(OBu)(O-2,6-tBu2-4-MeC6H2)-κO:κO']2[PO2(OBu)(O-2,6-tBu2-4-MeC6H2)-κO]2[HOPO(OBu)(O-2,6-tBu2-4-MeC6H2)-κO]2}·2C7H16, [Cr2(C19H32O4P)4(C19H33O4P)2(OH)2]·2C7H16, denoted (1)·2(heptane), [μ-bis(2,6-diisopropylphenyl) phosphato-1κO:2κO']bis[bis(2,6-diisopropylphenyl) phosphato]-1κO,2κO-chlorido-2κCl-triethanol-1κ2O,2κO-di-μ-ethanolato-1κ2O:2κ2O-dichromium(Cr-Cr) ethanol monosolvate or {Cr2(μ2-OEt)2[μ2-PO2(O-2,6-iPr2-C6H3)2-κO:κO'][PO2(O-2,6-iPr2-C6H3)2-κO]2Cl(EtOH)3}·EtOH, [Cr2(C2H5O)2(C24H34O4P)3Cl(C2H6O)3]·C2H6O, denoted (2)·EtOH, and di-μ-ethanolato-1κ2O:2κ2O-bis{[bis(2,6-diisopropylphenyl) hydrogen phosphato-κO][bis(2,6-diisopropylphenyl) phosphato-κO]chlorido(ethanol-κO)chromium}(Cr-Cr) benzene disolvate or {Cr2(μ2-OEt)2[PO2(O-2,6-iPr2-C6H3)2-κO]2[HOPO(O-2,6-iPr2-C6H3)2-κO]2Cl2(EtOH)2}·2C6H6, [Cr2(C2H5O)2(C24H34O4P)2(C24H35O4P)2Cl2(C2H6O)2]·2C6H6, denoted (3)·2C6H6. Complexes (1)-(3) have been synthesized by an exchange reaction between the in-situ-generated corresponding lithium or potassium disubstituted phosphates with CrCl3(H2O)6 in ethanol. The subsequent crystallization of (1) from heptane, (2) from ethanol and (3) from an ethanol/benzene mixture allowed us to obtain crystals of (1)·2(heptane), (2)·EtOH and (3)·2C6H6, whose structures have the monoclinic P21, orthorhombic P212121 and triclinic P-1 space groups, respectively. All three complexes have binuclear cores with a single Cr-Cr bond, i.e. Cr2O6P2 in (1), Cr2PO4 in (2) and Cr2O2 in (3), where the Cr atoms are in distorted octahedral environments, formally having 16 ē per Cr atom. The complexes have bridging ligands μ2-OH in (1) or μ2-OEt in (2) and (3). The organophosphate ligands demonstrate terminal κO coordination modes in (1)-(3) and bridging μ2-κO:κO' coordination modes in (1) and (2). All the complexes exhibit hydrogen bonding: two intramolecular Ophos...H-Ophos interactions in (1) and (3) form two {H[PO2(OR)2]2} associates; two intramolecular Cl...H-OEt hydrogen bonds additionally stabilize the Cr2O2 core in (3); two intramolecular Ophos...H-OEt interactions and two O...H-O intermolecular hydrogen bonds with a noncoordinating ethanol molecule are observed in (2)·EtOH. The presence of both basic ligands (OH- or OEt-) and acidic [H(phosphate)2]- associates at the same metal centres in (1) and (3) is rather unusual. Complexes may serve as precatalysts for ethylene polymerization under mild conditions, providing polyethylene with a small amount of short-chain branching. The formation of a small amount of α-olefins has been detected in this reaction.