Spectrophotometric determination of anthracycline anticancer agents with aluminum(III) and chromazurol S in a nonionic surfactant micellar medium.

A simple and highly sensitive spectrophotometric method for the determination of anthracycline anticancer agents, such as Daunorubicin hydrochloride (DAU), was established by using aluminum(III) and Chromazurol S (CAS) in a nonionic surfactant micellar medium. In the case of determination of DAU, the apparent molar absorptivity was 1.3 x 10(5) dm3 mol(-1) cm(-1) at 615 nm. Beer's law was obeyed in the concentration range of 0.028 - 2.82 microg ml(-1) for DAU. Owing to no need for solvent extraction, this method could be applied to assays of DAU and related drugs in pharmaceutical preparations.     

Free-fermions and skew stable Grothendieck polynomials

Journal of Algebraic Combinatorics - Motivated by the theory of correspondence functors, we introduce the notion of germ in a finite poset, and the notion of germ extension of a poset. We show that...     

Position — Sensitive single-wire proportional counter for conversion electron Mössbauer spectroscopy

A position-sensitive single-wire proportional counter for the INS 2 air-core spectrometer has been improved to take conversion electron Mössbauer spectrum as a function of electron energy with a multichannel mode. The position resolution at 13.6 keV was found to become 1.6 mm with the counter gas pressure of 320 Torr. The position resolution was obtained as a function of energy between 7 and 60 keV for gas pressure of 40 Torr, 160 Torr and 320 Torr. The L, M and N conversion electron spectrum of the 14.4 keV transition in⁵⁷Fe was taken with the present system. Overall momentum resolution was found to be 0.23% for the L₁-line and 0.19% for the M₁ line.     

Application of coset representations to the construction of symmetry adapted functions

Summary A coset representation (G(/G _i )), which is defined algebraically by a coset decomposition of a finite groupG by its subgroupG _i , is shown to be a method for the decomposition of a regular body into its point group orbits. This proof also shows that each member of theG(/G _i ) orbit belongs to theG _i site-symmetry. In addition, a general equation concerning the multiplicities of such coset representations is derived and shown to involve Brester's equations and thek-value equations of framework groups as special cases. The relationship of the coset representation and the site-symmetry affords a general procedure for obtaining symmetry adapted functions.     

Synthetic and structural studies of [6]-, [7]- and [10]metacyclophanes

A new preparative sequence from 2,3-polymethylene-2-cyclopentenone 5 to 2,6-polymethylenebromobenzenes 3 (n = 6, 7, 10) and 2,6-polymethylenephenyllithiums 6 has been found. The reaction of 6 with various electrophiles produces a number of new compounds to disclose the unique reactivity of the aryl C-Li moiety surrounded by the polymethylene chain. Photolysis of 3a and 3b provides transannular products 8, 10 and 11, all arising from the proximity between the aromatic bromine and the aliphatic hydrogen intraannularly opposed to be removed as HBr. Spectrometric study gives quantitative data of the dependence of the molecular geometry upon the chain length and the aromatic substituents. The energy barriers ΔG_c^≠ of the conformational flipping are 17·4 kcal/mol (T_c 76·5°) for [6]metacyclophane (7a), 11·5 kcal/mol (T_c ?28°) for [7]metacyclophane (7b), ·8 kcal/mol for [10]metacyclophane (7c). The lower-energy process of the aliphatic chain in [6]metacyclophane derivatives is the pseudorotation with substituent-dependent barrier ΔG_c^≠ 11·1 kcal/mol (T_c ?31·5°) for 7a, 12·4 kcal/mol (T_c ?4·5°) for 3a and 12·7 kcal/mol (T_c 1·0°) for 12a. The rather large rotational barrier is attributed to the compressed structure of each system. The benzene ring distortion of the cyclophanes is deduced from the bathochromic shift of the B-band and the diamagnetic shift of the benzene proton signals in the PMR.     

57Fe Mössbauer study under high pressure; ε-Fe and Fe2O3

Using diamond anvil cell, the⁵⁷Fe Mössbauer spectra of pure iron foil and α-Fe₂O₃ powder under high pressure have been measured at room temperature.⁵⁷Fe Mössbauer spectra of α-Fe were measured from 15 GPa to 45 GPa. Isomer shift value decreased and the quadrupole splitting slightly increased as the pressure increased.⁵⁷Fe Mössbauer spectra of Fe₂O₃ under high pressure up to 72 GPa were observed. Above 52 GPa, the new lines appeared at the center portion of the spectrum corresponding to the new high pressure phase. The spectrum of new high pressure phase consisted of 6-line splitting and doublet, suggesting the existence of the two different kinds of iron states in it.