鄭氏詩譜攷正 1巻. 詩攷補注 2巻補遺1巻. 毛鄭詩釋 3巻續錄1巻. 禮記釋注 4巻. 儀禮釋注 2巻. 周禮釋注 2巻

Mode of access: Internet.

草廬呉文正公全集 49巻首1巻外集3巻. 儀禮逸經 1巻. 葬書 1巻. 三禮考註64巻. 孝經 1巻. 春秋纂言 12巻總例2巻. 易纂言 12巻首1巻. 周易纂言外翼 8巻. 書經纂言 4巻. 學言稿 1巻

Mode of access: Internet.

The catholic doctrine of a Trinity : proved by above an hundred short and clear arguments, expressed in the terms of the Holy Scripture, compared in a manner entirely new and digested under the four following titles: 1. The divinity of Christ. 2. The divinity of the Holy Ghost. 3. The plurality of persons. 4. The Trinity in unity. With a few reflections, occasionally interspersed, upon some of the Arian writers, particularly Dr. S. Clarke: to which is added, A letter to the common people, in answer to some popular arguments against the Trinity.

A reply to "An appeal to the common sense of all Christian people", by William Hopkins.

Organizational maintenance manual : lathe, engine, bench mounted, solid bed type, 10 inch swing, no. 2 Morse taper center, 1-3/8 spindle hole, 110-volts, 60 cycle, single phase 3/4-horsepower, w/Army dwg. no. 7550151 bench (standard-modern tool series 2,000 model, 11 inch) (3416-517-0955).

"November 1965."

Uber 1.3-Diketo-2.4-tetrachlorhydronaphtalin und dessen Umwandlungsprodukte.

Thesis (doctoral)--Universitat Marburg.

Organic reactions in ionic liquids; Ionic liquid-accelerated three-component reaction: a rapid one-pot synthesis of 3-alkyl-5-[(Z)-arylmethylidene]-1,3-thiazolidine-2,4-diones

A rapid one-pot synthesis of 3-alkyl-5-[(Z)-arylme­thylidene]-1,3-thiazolidine-2,4-dionesis described that occurs in recyclable ionic liquid [bmim]PF6 (1-butyl-3-methylimidazolium hexafluorophosphate).Significant rate enhancement and good selectivity have been observed.

Use of a solvent-free dry matrix coating for quantitative matrix-assisted laser desorption ionization imaging of 4-bromophenyl-1,4-diazabicyclo(3.2.2)nonane-4-carboxylate in rat brain and quantitative analysis of the drug from laser microdissected tissue regions

A dry matrix application for matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) was used to profile the distribution of 4-bromophenyl-1,4-diazabicyclo(3.2.2)nonane-4-carboxylate, monohydrochloride (BDNC, SSR180711) in rat brain tissue sections. Matrix application involved applying layers of finely ground dry alpha-cyano-4-hydroxycinnamic acid (CHCA) to the surface of tissue sections thaw mounted onto MALDI targets. It was not possible to detect the drug when applying matrix in a standard aqueous-organic solvent solution. The drug was detected at higher concentrations in specific regions of the brain, particularly the white matter of the cerebellum. Pseudomultiple reaction monitoring imaging was used to validate that the observed distribution was the target compound. The semiquantitative data obtained from signal intensities in the imaging was confirmed by laser microdissection of specific regions of the brain directed by the imaging, followed by hydrophilic interaction chromatography in combination with a quantitative high-resolution mass spectrometry method. This study illustrates that a dry matrix coating is a valuable and complementary matrix application method for analysis of small polar drugs and metabolites that can be used for semiquantitative analysis.

Understanding the twist-bend nematic phase: the characterisation of 1-(4-cyanobiphenyl-4'-yloxy)-6-(4-cyanobiphenyl-4'-yl) hexane (CB6OCB) and comparison with CB7CB

Acknowledgements The FFTEM data were obtained at the (Cryo) TEM facility at the Liquid Crystal Institute, Kent State University, supported by the Ohio Research Scholars Program Research Cluster on Surfaces in Advanced Materials. ODL acknowledges the support of NSF DMR-1410378 grant. The authors are grateful for financial support from MINECO/FEDER MAT2015-66208-C3-2-P and from the Gobierno Vasco (GI/IT-449-10)

Coordination networks of Cu2+ ions with 1,3-bis[2-(4-pyridyl)ethyl]benzene : strong structure-directing role of the counter ion (nitrate, acetate and sulphate), leading to clusters, sheets and chains

Date of Acceptance: 16/10/2015