𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Vibrational spectroscopic study of H-CC-H2-O-P(S)Cl2

✍ Scribed by R.A. Nyquist; W.W. Muelder


Publisher
Elsevier Science
Year
1968
Tongue
English
Weight
802 KB
Volume
2
Category
Article
ISSN
0022-2860

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Toward the spectroscopic identification
✍ Yoshihiro Osamura; Henry F. Schaefer III 📂 Article 📅 1981 🏛 Elsevier Science 🌐 English ⚖ 319 KB

The smglet electromc ground state of vmyhdene WIU be very dtfficult to observe spectroscopically, as It rapldly tunnels througfi a small (6 kcal mol-'1 barner to acetylene TrIplet vmyhdene should have a much longer hfetune, and several prelctlons of Its PropertIes are reported here These mclude the

Infrared spectra of matrix-isolated prop
✍ Eiichi Suzuki; Fumio Watari 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 278 KB

Pyrolysis (900 K) of cyclopenteno-1.2,3-thiadiazole with trapping of the products in argon at 20 K gave ethylene and propadienethione. Small quantities of thioketene and trimethylenethioketene were also formed. The infrared bands due to propadienethione were identified by their disappearance on irra

Theoretical studies of the radical react
✍ Shogo Sakai; Mark S. Gordon 📂 Article 📅 1986 🏛 Elsevier Science 🌐 English ⚖ 351 KB

Ab initio molecular orbltal calculations on the transitton states and barrter heights for the addition of atomtc hydrogen to sllaethylene are carried out. The activation energy for the addition to the silicon site is lower than that to the carbon site, wlnle the exothermicity 1s smaller.

Theoretical study of the CH bond dissoc
✍ Charles W. Bauschlicher Jr.; Stephen R. Langhoff 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 554 KB

The successive C-H bond dissociation energies of CH,, &Hz. C2H4, and H&O (ketene) are determined using large basis sets and a high level of correlation treatment. For CHI, C2H2, and C2H4 the computed values are in excellent agreement with experiment. Using our results we recommend 107.9 +2.0 and 96.