The yield on China 10Y Bond Yield eased to 1.65% on July 1, 2025, marking a 0 percentage point decrease from the previous session. Over the past month, the yield has fallen by 0.05 points and is 0.59 points lower than a year ago, according to over-the-counter interbank yield quotes for this government bond maturity. China 10-Year Government Bond Yield - values, historical data, forecasts and news - updated on July of 2025.

Turkey Internet Banking: FT: IN: Value: Bonds and Bills: Sell data was reported at 3,058.922 TRY mn in Jun 2018. This records an increase from the previous number of 1,439.745 TRY mn for Mar 2018. Turkey Internet Banking: FT: IN: Value: Bonds and Bills: Sell data is updated quarterly, averaging 217.529 TRY mn from Mar 2007 (Median) to Jun 2018, with 46 observations. The data reached an all-time high of 3,058.922 TRY mn in Jun 2018 and a record low of 112.608 TRY mn in Mar 2013. Turkey Internet Banking: FT: IN: Value: Bonds and Bills: Sell data remains active status in CEIC and is reported by The Banks Association of Turkey. The data is categorized under Global Database’s Turkey – Table TR.KA010: Internet Banking Statistics.

3 Ft Bond Index curve from Halliburton Logging. Measured in unitless.

Turkey Internet Banking: FT: IN: Vol: Bonds and Bills: Sell data was reported at 66.935 Unit th in Jun 2018. This records an increase from the previous number of 44.895 Unit th for Mar 2018. Turkey Internet Banking: FT: IN: Vol: Bonds and Bills: Sell data is updated quarterly, averaging 29.980 Unit th from Mar 2007 (Median) to Jun 2018, with 46 observations. The data reached an all-time high of 66.935 Unit th in Jun 2018 and a record low of 14.571 Unit th in Dec 2016. Turkey Internet Banking: FT: IN: Vol: Bonds and Bills: Sell data remains active status in CEIC and is reported by The Banks Association of Turkey. The data is categorized under Global Database’s Turkey – Table TR.KA010: Internet Banking Statistics.

Turkey Internet Banking: FT: IN: Vol: Bonds and Bills: Buy data was reported at 50.331 Unit th in Mar 2018. This records an increase from the previous number of 43.341 Unit th for Dec 2017. Turkey Internet Banking: FT: IN: Vol: Bonds and Bills: Buy data is updated quarterly, averaging 50.331 Unit th from Mar 2007 (Median) to Mar 2018, with 45 observations. The data reached an all-time high of 179.760 Unit th in Mar 2007 and a record low of 20.847 Unit th in Sep 2016. Turkey Internet Banking: FT: IN: Vol: Bonds and Bills: Buy data remains active status in CEIC and is reported by The Banks Association of Turkey. The data is categorized under Global Database’s Turkey – Table TR.KA010: Internet Banking Statistics.

This dataset provides information about the number of properties, residents, and average property values for Bonds Ranch Road cross streets in Fort Worth, TX.

Internet Banking: FT: IN: Value: Bonds and Bills data was reported at 6,508.864 TRY mn in Jun 2018. This records an increase from the previous number of 3,260.748 TRY mn for Mar 2018. Internet Banking: FT: IN: Value: Bonds and Bills data is updated quarterly, averaging 1,123.525 TRY mn from Mar 2007 (Median) to Jun 2018, with 46 observations. The data reached an all-time high of 6,508.864 TRY mn in Jun 2018 and a record low of 451.499 TRY mn in Sep 2016. Internet Banking: FT: IN: Value: Bonds and Bills data remains active status in CEIC and is reported by The Banks Association of Turkey. The data is categorized under Global Database’s Turkey – Table TR.KA010: Internet Banking Statistics.

data for the figure

Link to the ScienceBase Item Summary page for the item described by this metadata record. Service Protocol: Link to the ScienceBase Item Summary page for the item described by this metadata record. Application Profile: Web Browser. Link Function: information

Single crystals of orthorhombic l-arginine formate (+(NH2)2CNH(CH2)3CH(NH3+)COO-·HCOO-) that had dimensions of ca. 30 × 30 × 40 mm and were of optical quality were grown by controlled evaporation of aqueous solutions. An X-ray structure analysis yielded space group P212121, a1 = 7.706(2) Å, a2 = 7.808(2) Å, a3 = 18.594(4) Å, Z = 4, and ρc = 1.308 Mg/m3 at 293 K. Hydrogen bonds determine the interactions between monovalent l-arginine cations and also the interactions of these cations with formate anions. The structure is compared with that of the monoclinic polymorph. ATR FTIR and FT Raman spectra, TG, DTA, thermal expansion, and elastic and thermoelastic properties are reported.

The gallium(III)-containing heteropolytungstates [Ga4(H2O)10(β-XW9O33)2]6– (X = AsIII, 1; SbIII, 2) were synthesized in aqueous acidic medium by reaction of Ga3+ ions with the trilacunary, lone-pair-containing [XW9O33]9–. Polyanions 1 and 2 are isostructural and crystallized as the hydrated sodium salts Na6[Ga4(H2O)10(β-AsW9O33)2]·28H2O (Na-1) and Na6[Ga4(H2O)10(β-SbW9O33)2]·30H2O (Na-2) in the monoclinic space group P21/c, with unit cell parameters a = 16.0218(12) Å, b = 15.2044(10) Å, c = 20.0821(12) Å, and β = 95.82(0)°, as well as a = 16.0912(5) Å, b = 15.2178(5) Å, c = 20.1047(5) Å, and β = 96.2(0)°, respectively. The corresponding tellurium(IV) derivative [Ga4(H2O)10(β-TeW9O33)2]4– (3) was also prepared, by direct reaction of sodium tungstate, tellurium(IV) oxide, and gallium nitrate. Polyanion 3 crystallized as the mixed rubidium/sodium salt Rb2Na2[Ga4(H2O)10(β-TeW9O33)2]·28H2O (RbNa-3) in the triclinic space group P1̅ with unit cell parameters a = 12.5629(15) Å, b = 13.2208(18) Å, c = 15.474(2) Å, α = 80.52(1)°, β = 84.37(1)°, and γ = 65.83(1)°. All polyanions 1–3 were characterized in the solid state by single-crystal XRD, FT-IR, TGA, and elemental analysis, and polyanion 2 was also characterized in solution by 183W NMR and UV–vis spectroscopy. Polyanion 2 was used as a homogeneous catalyst toward adenosine triphosphate (ATP) and the DNA model substrate 4-nitrophenylphosphate, monitored by 1H and 31P NMR spectroscopy. The encapsulated gallium(III) centers in 2 promote the Lewis acidic synergistic activation of the hydrolysis of ATP and DNA model substrates at a higher rate in near-physiological conditions. A strong interaction of 2 with the P–O bond of ATP was evidenced by changes in chemical shift values and line broadening of the 31P nucleus in ATP upon addition of the polyanion.

Link to the ScienceBase Item Summary page for the item described by this metadata record. Service Protocol: Link to the ScienceBase Item Summary page for the item described by this metadata record. Application Profile: Web Browser. Link Function: information

网上银行：FT：IN：量：债券和票据：买入在03-01-2018达50.331千站，相较于12-01-2017的43.341千站有所增长。网上银行：FT：IN：量：债券和票据：买入数据按季更新，03-01-2007至03-01-2018期间平均值为50.331千站，共45份观测结果。该数据的历史最高值出现于03-01-2007，达179.760千站，而历史最低值则出现于09-01-2016，为20.847千站。CEIC提供的网上银行：FT：IN：量：债券和票据：买入数据处于定期更新的状态，数据来源于Türkiye Bankalar Birliği，数据归类于全球数据库的土耳其 – 表 TR.KA010：网上银行统计。

Savannah Bond d 6 Haziran 1990 Melbourne Victoria Avustralyalı pornografik film oyuncusu Savannah BondDoğum6 Haziran 199

This is the raw data of Fourier Infrared (FT-IR) spectral analysis.

The attempt to prepare hitherto unknown homopolyatomic cations of sulfur by the reaction of elemental sulfur with blue S8(AsF6)2 in liquid SO2/SO2ClF, led to red (in transmitted light) crystals identified crystallographically as S8(AsF6)2. The X-ray structure of this salt was redetermined with improved resolution and corrected for librational motion:  monoclinic, space group P21/c (No. 14), Z = 8, a = 14.986(2) Å, b = 13.396(2) Å, c = 16.351(2) Å, β = 108.12(1)°. The gas phase structures of E82+ and neutral E8 (E = S, Se) were examined by ab initio methods (B3PW91, MPW1PW91) leading to ΔfH⊖[S82+, g] = 2151 kJ/mol and ΔfH⊖[Se82+, g] = 2071 kJ/mol. The observed solid state structures of S82+ and Se82+ with the unusually long transannular bonds of 2.8−2.9 Å were reproduced computationally for the first time, and the E82+ dications were shown to be unstable toward all stoichiometrically possible dissociation products En+ and/or E42+ [n = 2−7, exothermic by 21−207 kJ/mol (E = S), 6−151 kJ/mol (E = Se)]. Lattice potential energies of the hexafluoroarsenate salts of the latter cations were estimated showing that S8(AsF6)2 [Se8(AsF6)2] is lattice stabilized in the solid state relative to the corresponding AsF6- salts of the stoichiometrically possible dissociation products by at least 116 [204] kJ/mol. The fluoride ion affinity of AsF5(g) was calculated to be 430.5 ± 5.5 kJ/mol [average B3PW91 and MPW1PW91 with the 6-311+G(3df) basis set]. The experimental and calculated FT-Raman spectra of E8(AsF6)2 are in good agreement and show the presence of a cross ring vibration with an experimental (calculated, scaled) stretching frequency of 282 (292) cm-1 for S82+ and 130 (133) cm-1 for Se82+. An atoms in molecules analysis (AIM) of E82+ (E = S, Se) gave eight bond critical points between ring atoms and a ninth transannular (E3−E7) bond critical point, as well as three ring and one cage critical points. The cage bonding was supported by a natural bond orbital (NBO) analysis which showed, in addition to the E8 σ-bonded framework, weak π bonding around the ring as well as numerous other weak interactions, the strongest of which is the weak transannular E3−E7 [2.86 Å (S82+), 2.91 Å (Se82+)] bond. The positive charge is delocalized over all atoms, decreasing the Coulombic repulsion between positively charged atoms relative to that in the less stable S8-like exo−exo E82+ isomer. The overall geometry was accounted for by the Wade−Mingos rules, further supporting the case for cage bonding. The bonding in Te82+ is similar, but with a stronger transannular E3−E7 (E = Te) bonding. The bonding in E82+ (E = S, Se, Te) can also be understood in terms of a σ-bonded E8 framework with additional bonding and charge delocalization occurring by a combination of transannular nπ*−nπ* (n = 3, 4, 5), and np2 → nσ* bonding. The classically bonded S82+ (Se82+) dication containing a short transannular S+−S+ (Se+−Se+) bond of 2.20 (2.57) Å is 29 (6) kJ/mol higher in energy than the observed structure in which the positive charge is delocalized over all eight chalcogen atoms.

Three five-coordinate high-spin (cyano)manganese(II) complexes, utilized tetraphenylporphyrin (TPP), tetratolylporphyrin (TTP), and tetramesitylporphyrin (TMP) as ligands, are prepared and studied by single-crystal X-ray, FT-IR, UV–vis, and EPR spectroscopies. The crystal structure studies revealed noteworthy structural features including unexpectedly wide tilting angles of the axial Mn–CCN bonds, which is contrasted to the isoelectronic Fe(III)–CCN bonds. Solid-state EPR measurements (90 K) and simulations are applied to obtain the ZFS parameters (D, E, and E/D (λ)), which are compared to Mn(II) porphyrin analogues of hemes to understand the ligand field of the cyanide. The solution EPR studies gave new insights into the chemical equilibrium of four- and five-coordinate species, which has been monitored by UV–vis spectroscopy.