The group 5 mixed-metal telluride, Hf(0.78)Ti(0.22)Te(5) (hafnium titanium penta-telluride), is isostructural with the binary phases HfTe(5) and ZrTe(5) and forms a layered structure extending parallel to (010). The layers are made up from chains of bicapped metal-centered trigonal prisms and zigzag Te chains. The metal site (site symmetry m2m) is occupied by statistically disordered Hf [78.1 (5)%] and Ti [21.9 (5)%]. In addition to the regular Te-Te pair [2.7448 (13) Å] forming the short base of the equilateral triangle of the trigonal prism, an inter-mediate Te⋯Te separation [2.9129 (9) Å] is also found. The classical charge balance of the compound can be described as [M(4+)][Te(2-)][Te(2) (2-)][Te(2) (0)] (M = Hf, Ti). The individual metal content can vary in different crystals, apparently forming a random substitutional solid solution (Hf(1-x)Ti(x))Te(5), with 0.15 ≤ x ≤ 0.22.
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http://dx.doi.org/10.1107/S1600536812006691 | DOI Listing |
Acta Crystallogr Sect E Struct Rep Online
March 2012
Division of Energy Systems Research and Department of Chemistry, Ajou University, Suwon 443-749, Republic of Korea.
The group 5 mixed-metal telluride, Hf(0.78)Ti(0.22)Te(5) (hafnium titanium penta-telluride), is isostructural with the binary phases HfTe(5) and ZrTe(5) and forms a layered structure extending parallel to (010).
View Article and Find Full Text PDFWorld J Gastroenterol
October 2004
Department of Infectious Diseases, Zhongshan People's Hospital, Zhongshan 528400, Guangdong Providence, China.
Aim: To design and construct an exogenous multiple epitope of helper T lymphocytes (HTL), and to evaluate its effect on anti-HBs response through DNA immunization.
Methods: Artificial HTL epitope, PADRE and four other HTL epitopes from different proteins were linked together using splicing by overlap extension to generate exogenous multiple epitopes of HTL, MTE5. pcMTE5 and pcHB were generated by cloning MTE5 and fragments of HBV pre-S2/S gene into mammalian expression plasmid pcDNA3.
Zhonghua Yi Xue Za Zhi
February 2003
Department of Infectious Diseases, Third Affiliated Hospital, Zhongshan University, Guangzhou 510630, China.
Objective: To study the effect of exogenous epitope of helper T lymphocyte (HTL) on humoral immunity of HBV S gene DNA immunity.
Methods: Two universal HTL epitopes, amino acid residue (aa) 830-843 of the tetanus toxoid (TTE) and artificial epitope (PADRE), and 3 unique epitopes, aa1-20 of tubercle bacteria hot shock protein 65 (TBE), aa54-65 of rubella protein E2-4 (ME) and aa35-48 of trachoma hot shock protein 60 (CE) were chosen. Eukaryotic expression vectors were constructed by inserting single or multiple exogenous epitopes in HBV S gene just after the initial code of translation.
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