𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and X-Ray Structure Analysis of anti-1-Bromotricyclo[5.1.0.03,5]octane-2,6-dione (anti-1-Bromobishomoquinone)

✍ Scribed by Dipl.-Chem. Jürg Heller; Prof. Dr. André S. Dreiding; Dr. Rita Grieb; Prof. Dr. Alfred Niggli

Publisher
John Wiley and Sons
Year
1972
Tongue
English
Weight
301 KB
Volume
11
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthese und Röntgen-Strukturanalyse von
Synthese und Röntgen-Strukturanalyse von anti-1-Brom-tricyclo[5.1.0.03,5]octan-2,6-dion (anti-1-Brom-bishomochinon)
✍ Dipl.-Chem. Jürg Heller; Prof. Dr. André S. Dreiding; Dr. Rita Grieb; Prof. Dr. 📂 Article 📅 1972 🏛 John Wiley and Sons 🌐 English ⚖ 292 KB

ven JT-Komponenten der ersten Bande (a. 0.4eV; die dritte Komponente laDt sich im gespreizten Spektrum bei ca. 11.7 eV erkennen) ist kleiner als die in der ersten Bande des Methans gefundene (ca. 0.7 eVI5]); dies diirfte auf die im Neopentan verringerte Repulsion zwischen benachbarten CC-EOs zuruckz

Synthesis and Crystal Structure of (Sr1−
Synthesis and Crystal Structure of (Sr1−xLa1+x)Zn1−xO3.5−x/2(0.01≤x<0.03)
✍ Hisanori Yamane; Haruya Hara; Shun-ichi Kubota; Masahiko Shimada; Yasuo Yamaguch 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 469 KB

Sr 1؊x La 1؉x )Zn 1؊x O 3.5؊x/2 (0.014 4x < 0.03), was prepared at 1373 K in the SrO+La 2 O 3 +ZnO system. The X-ray and neutron powder di4raction peaks were indexed with a body-centered tetragonal unit cell (a ‫؍‬ 3.75 and c ‫؍‬ 13.57 A s for the sample x ‫؍‬ 0.01). Weak di4use superstructure re6ec

X-Ray Structure Analysis of 6-Thiatetrac
X-Ray Structure Analysis of 6-Thiatetracyclo-[5.4.0.02.4.03.5]undeca-1(7),8,10-triene
✍ Dr. Chizuko Kabuto; Dipl.-Chem. Toshio Tatsuoka; Prof. Dr. Ichiro Murata; Prof. 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 English ⚖ 225 KB 👁 1 views

Arsabenzene-4-carbaldehyde ( 4 ) can be obtained pure as a pale yellow oil by bulb tube vacuum distillation (10-' torr). Surprisingly, the product, which is stable under nitrogen, smells strongly and unmistakably of benzaldehyde, thus providing further justification for the trivial name "arsabenzald