HPt
- Formula: HPt
- Molecular weight: 196.092
- CAS Registry Number: 13966-55-7
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Reaction thermochemistry data
Go To: Top, Constants of diatomic molecules, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: John E. Bartmess
Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.
Individual Reactions
Pt- + = HPt
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 344.89 | kcal/mol | D-EA | Bilodeau, Scheer, et al., 1999 | gas phase |
Constants of diatomic molecules
Go To: Top, Reaction thermochemistry data, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Klaus P. Huber and Gerhard H. Herzberg
Data collected through May, 1975
Symbol | Meaning |
---|---|
State | electronic state and / or symmetry symbol |
Te | minimum electronic energy (cm-1) |
ωe | vibrational constant – first term (cm-1) |
ωexe | vibrational constant – second term (cm-1) |
ωeye | vibrational constant – third term (cm-1) |
Be | rotational constant in equilibrium position (cm-1) |
αe | rotational constant – first term (cm-1) |
γe | rotation-vibration interaction constant (cm-1) |
De | centrifugal distortion constant (cm-1) |
βe | rotational constant – first term, centrifugal force (cm-1) |
re | internuclear distance (Å) |
Trans. | observed transition(s) corresponding to electronic state |
ν00 | position of 0-0 band (units noted in table) |
State | Te | ωe | ωexe | ωeye | Be | αe | γe | De | βe | re | Trans. | ν00 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
IV (2Σ) 2 | [2051] H | 8.03 | 0.40 | [4.4E-4] 1 | 1.447 | IV ← III R | 36504 H | |||||
↳Scullman, 1971 | ||||||||||||
III (2Σ) 2 | [9.51] | [3.7E-4] | [1.330] | |||||||||
II (2Σ) 2 | [5.22] | [4.1E-4] | [1.795] | II ← I R | 30311 H | |||||||
↳Scullman, 1971 | ||||||||||||
I (2Σ) 2 | [7.13] | [2.8E-4] | [1.536] | |||||||||
B (2Δ)5/2 | (26962) | [1548.18] 3 Z | (80) 4 | 6.003 5 6 | 0.301 | [3.15E-4] 7 | 1.6736 | B ↔ X1 R | 26613.91 3 Z | |||
↳Loginov, 1964; missing citation; Loginov, 1966; Kaving and Scullman, 1971 | ||||||||||||
State | Te | ωe | ωexe | ωeye | Be | αe | γe | De | βe | re | Trans. | ν00 |
B' (2Φ)7/2 | (24218) | [1428.7] 3 Z | (74) | 5.758 | 0.326 8 | [3.6E-4] 9 | 1.7088 | B' → X1 R | 23806.48 3 Z | |||
↳missing citation | ||||||||||||
A (2Δ)5/2 | (22311) | 1690.6 3 Z | 55.3 10 | -3.88 | [5.534] 11 | 12 | [3.55E-4] 13 | [1.7430] | A ↔ X1 R | 21960.59 3 Z | ||
↳Loginov, 1964; Neuhaus and Scullman, 1964; missing citation; Kaving and Scullman, 1971 | ||||||||||||
A' (2Δ)3/2 | (x2 + 19938) | [1500.08] 3 Z | (58) | 6.1103 14 | 0.2869 | [4.717E-4] 15 | 1.65879 | A' ↔ X2 R | 19610.82 3 Z | |||
↳missing citation | ||||||||||||
X2 (2Δ)3/2 | x2 16 | [2177.31] 3 Z | (43) | 7.2784 14 | 0.2029 | [2.834E-4] 17 | 1.51987 | |||||
State | Te | ωe | ωexe | ωeye | Be | αe | γe | De | βe | re | Trans. | ν00 |
X1 (2Δ)5/2 | 0 18 | [2294.68] 3 Z | (46) | 7.1963 | 0.1996 | [2.613E-4] 19 | 1.52852 |
Notes
1 | D1 = 4.9E-4. |
2 | Preliminary data only. |
3 | Band origins in the tables for PtH and PtD correspond to the energy of J'=0 relative to J"=0. Vibrational constants recalculated accordingly. |
4 | From the corresponding value for PtD. |
5 | Perturbations in both v=0 and v=1. |
6 | Predissociation above v=0, J=12.5, see Kaving and Scullman, 1971. |
7 | D1 = 3.94E-4. |
8 | Perturbation in v=1 at J~6.5, see Scullman, 1971. |
9 | D1 = 3.5E-4. |
10 | (v=0, ..., 3). |
11 | Ω-type doubling; for details see Scullman, 1965, Kaving and Scullman, 1971, Kaving and Scullman, 1974. |
12 | B1= 5.244, B2= 4.924, B3= 4.517 (v=3 perturbed for J ≥ 10.5). |
13 | D1(E-4 cm-1)= 3.68, D2(E-4 cm-1)= 4.42, D3(E-4 cm-1)= 8.8. |
14 | Ω-type doubling; see Kaving and Scullman, 1971. |
15 | D1 = 6.08E-4. |
16 | x2 ~1320; see Kaving and Scullman, 1971. |
17 | D1 = 2.84E-4 |
18 | Not certain that this is the ground state. |
19 | D1 = 2.607E-4. |
20 | From the predissociation in v=0 of B (2Δ)5/2, assuming that X1 is the ground state. |
References
Go To: Top, Reaction thermochemistry data, Constants of diatomic molecules, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Bilodeau, Scheer, et al., 1999
Bilodeau, R.C.; Scheer, M.; Haugen, H.K.; Brooks, R.L.,
Near-threshold Laser Spectroscopy of Iridium and Platinum Negative Ions: Electron Affinities and the Threshold Law,
Phys. Rev. A, 1999, 61, 1, 12505, https://doi.org/10.1103/PhysRevA.61.012505
. [all data]
Scullman, 1971
Scullman,
Dissertation, see USIP Report 71-02, Stockholm, 1971, 1. [all data]
Loginov, 1964
Loginov, V.A.,
The production of electronic band spectra by the exploding wire method,
Opt. Spectrosc. Engl. Transl., 1964, 16, 220, In original 402. [all data]
Loginov, 1966
Loginov, V.A.,
Absorption spectra of PtH and PtD,
Opt. Spectrosc. Engl. Transl., 1966, 20, 88, In original 167. [all data]
Kaving and Scullman, 1971
Kaving, B.; Scullman, R.,
Two new subsystems of PtH in the region 3500-5800 Å,
Can. J. Phys., 1971, 49, 2264. [all data]
Neuhaus and Scullman, 1964
Neuhaus, H.; Scullman, R.,
Das Bandenspektrum des PtH und PtD,
Z. Naturforsch. A, 1964, 19, 659. [all data]
Scullman, 1965
Scullman, R.,
Rotational analysis of violet and green bands of PtH,
Ark. Fys., 1965, 28, 255. [all data]
Kaving and Scullman, 1974
Kaving, B.; Scullman, R.,
Rotational analysis of the A2Δ5/2-X2Δ5/2 and B2Δ5/2 - X2Δ5/2 band sub-system of PtD,
Phys. Scr., 1974, 9, 33. [all data]
Notes
Go To: Top, Reaction thermochemistry data, Constants of diatomic molecules, References
- Symbols used in this document:
ΔrH° Enthalpy of reaction at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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