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Journal ArticleDOI

ORTEP-3 for Windows - a version of ORTEP-III with a Graphical User Interface (GUI)

Louis J. Farrugia
- 01 Oct 1997 - 
- Vol. 30, Iss: 5, pp 565-565
TLDR
L Lists of software presented and~or reviewed in the Journal of Applied Crystallography are available on the World Wide Web at the above address, together with information about the availability of the software where this is known.
Abstract
Computer Program Abstracts The category Computer Program Abstracts provides a rapid means of communicating up-to-date information concerning both new programs or systems and significant updates to existing ones. Following normal submission, a Computer Program Abstract will be reviewed by one or two members of the IUCr Commission on Crystallographic Computing. It should not exceed 500 words in length and should follow the standard format given on page 189 of the June 1985 issue of the Journal [J. Appl. CrysL (1985). 18, 189190] and on the World Wide Web at http://www.iucr. ac. uk/journals/jac/software/. Lists of software presented and~or reviewed in the Journal of Applied Crystallography are available on the World Wide Web at the above address, together with information about the availability of the software where this is known. J. App/. CrysL (1997). 30, 565 ORTEP-3 for Windows a version of ORTEP-III with a Graphical User Interface (GUI)

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Antiproliferative activity of chelating N,O- and N,N-ruthenium(II) arene functionalised poly(propyleneimine) dendrimer scaffolds

TL;DR: Chelating neutral and cationic first- and second-generation ruthenium(II) arene metallodendrimers based on poly(propyleneimine) dendrimer scaffolds and related mononuclear complexes, which established cytotoxicities of the mono- and multinuclear complexes were established using human ovarian carcinoma cancer cell lines.
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Iron chelators of the dipyridylketone thiosemicarbazone class: precomplexation and transmetalation effects on anticancer activity.

TL;DR: The divalent Mn(II), Ni, Cu, and Zn(II) complexes of the HDpT analogues are equally active in preventing proliferation as their ligands, suggesting the complexes act as lipophilic vehicles facilitating intracellular delivery of the free ligand upon metal dissociation.
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Electronic tuning of the lability of Pt(II) complexes through π-acceptor effects. Correlations between thermodynamic, kinetic, and theoretical parameters

TL;DR: DFT calculations at the B3LYP/LACVP level of theory show that, by the addition of pi-acceptor ligands to the metal, the positive charge on the metal center increases, and the energy separation of the frontier molecular orbitals of the ground state Pt(II) complexes decreases.
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Net Oxidative Addition of C(sp3)-F Bonds to Iridium via Initial C-H Bond Activation

TL;DR: The addition of C(sp3)-F bonds (including alkyl-F) to an iridium center via the initial, reversible cleavage of a C-H bond is reported, suggesting a distinct strategy for the development of catalysts and promoters to make and break C-F bonds.
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Possible steric control of the relative strength of chelation enhanced fluorescence for zinc(II) compared to cadmium(II): metal ion complexing properties of tris(2-quinolylmethyl)amine, a crystallographic, UV-visible, and fluorometric study.

TL;DR: The observation that, as expected, the CHEF effect in the Zn(II)/TQA complex is much stronger than that in the Cd(II/T QA complex, in contrast to similar but more sterically crowded ligands, where theCHEF effect is stronger in theCd( II) complex.
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