Report of the Department of Labor and Printing of the State of North Carolina [serial].

Report for 1926-1928 not issued.

Memorie istoriche di Ferdinando I, re del Regno delle Due Sicilie /

Mode of access: Internet.

Omaggio funebre alla memoria di Ferdinando I, re del regno delle due Sicilie.

Mode of access: Internet.

Elogio funebre alla gloriosa memoria di Ferdinando I, re del regno delle due Sicilie, ne'funerali a proprie spese celebrati nel di 16 gennaro dell'anno 1825 ... /

Mode of access: Internet.

Iscrizioni ed orazione nei solenni funerali di S.M. Ferdinando I, re del regno delle due Sicilie, nel dì 27 gennajo 1825 /

Mode of access: Internet.

Ne'funerali solenni per sua S.R.M. Ferdinando I, re del regno delle due Sicilie, celebrati nella cappella del Tesoro di S. Gennaro dalla Real Deputazione della medesima a'24 gennajo 1825 : orazione /

Mode of access: Internet.

Elogio ne'funerali di Ferdinando I, re del regno delle due Sicilie, celerrati nella chiesa del Purgatorio ad arco nel dì 18 febrajo /

Mode of access: Internet.

Per le nozze di sua maestà il re del regno delle due Sicilie Ferdinando II con Maria Cristina di Savoia : componimenti recitati il dì 9 dicembre 1832 in casa del conte D. Luigi Gaetani.

Mode of access: Internet.

A history of the University of South Carolina,

Mode of access: Internet.

History of the South Carolina college, from its incorporation, Dec. 19, 1801, to Dec. 19, 1865,

Mode of access: Internet.

Annual report of the State Board of Health of South Carolina.

Title varies slightly.

The origin of the difference in the superconducting critical temperatures of the beta(H) and beta(L) phases of (BEDT-TTF)(2)I-3

Incommensurate lattice fluctuations are present in the beta(L) phase (T-c similar to 1.5 K) of ET2I3 (where ET is BEDT-TTF - bis(ethylenedithio)tetrathiafulvalene) but are absent in the beta(H) phase (T-c similar to 7 K). We propose that the disorder in the conformational degrees of freedom of the terminal ethylene groups of the ET molecules, which is required to stabilise the lattice fluctuations, increases the quasiparticle scattering rate and that this leads to the observed difference in the Superconducting critical temperatures, T-c, of the two phases. We calculate the dependence of T-c on the interlayer residual resistivity. Our theory has no free parameters. Our predictions are shown to be consistent with experiment. We describe experiments to conclusively test our hypothesis.

Interim report of the South Carolina State Health and Human Services Finance Commission

This report summarizes the Commission's activities through June 30, 1984.

ANNUAL REPORT OF THE SOUTH CAROLINA COMMISSION FOR THE BLIND FOR THE FISCAL YEAR 1974-1975

The South Carolina Commission for the Blind reports to the Office of the Governor its annual report that includes summaries, financial statements, organizational charts, and directories.

Proton-transfer versus nontransfer in compounds of the diazo-dye precursor 4-(phenyldiazenyl) aniline (aniline yellow) with strong organic acids: the 5-sulfosalicylate and the dichroic benzenesulfonate salts, and the 1:2 adduct with 3,5-dinitrobenzoic

The structures of two 1:1 proton-transfer red-black dye compounds formed by reaction of aniline yellow [4-(phenyldiazenyl)aniline] with 5-sulfosalicylic acid and benzenesulfonic acid, and a 1:2 nontransfer adduct compound with 3,5-dinitrobenzoic acid have been determined at either 130 or 200 K. The compounds are 2-(4-aminophenyl)-1-phenylhydrazin-1-ium 3-carboxy-4-hydroxybenzenesulfonate methanol solvate, C12H12N3+.C7H5O6S-.CH3OH (I), 2-(4-aminophenyl)-1-hydrazin-1-ium 4-(phenydiazinyl)anilinium bis(benzenesulfonate), 2C12H12N3+.2C6H5O3S-, (II) and 4-(phenyldiazenyl)aniline-3,5-dinitrobenzoic acid (1/2) C12H11N3.2C~7~H~4~N~2~O~6~, (III). In compound (I) the diaxenyl rather than the aniline group of aniline yellow is protonated and this group subsequently akes part in a primary hydrogen-bonding interaction with a sulfonate O-atom acceptor, producing overall a three-dimensional framework structure. A feature of the hydrogen bonding in (I) is a peripheral edge-on cation-anion association involving aromatic C--H...O hydrogen bonds, giving a conjoint R1/2(6)R1/2(7)R2/1(4)motif. In the dichroic crystals of (II), one of the two aniline yellow species in the asymmetric unit is diazenyl-group protonated while in the other the aniline group is protonated. Both of these groups form hydrogen bonds with sulfonate O-atom acceptors and thee, together with other associations give a one-dimensional chain structure. In compound (III), rather than proton-transfer, there is a preferential formation of a classic R2/2(8) cyclic head-to-head hydrogen-bonded carboxylic acid homodimer between the two 3,5-dinitrobenzoic acid molecules, which in association with the aniline yellow molecule that is disordered across a crystallographic inversion centre, result in an overall two-dimensional ribbon structure. This work has shown the correlation between structure and observed colour in crystalline aniline yellow compounds, illustrated graphically in the dichroic benzenesulfonate compound.