Selected ATcT [1, 2] enthalpy of formation based on version 1.122 of the Thermochemical Network [3]This version of ATcT results was partially described in Ruscic et al. [4], and was also used for the initial development of highaccuracy ANLn composite electronic structure methods [5]. 

 
Representative Geometry of Kr+ (g)  
spin ON spin OFF  
Top contributors to the provenance of Δ_{f}H° of Kr+ (g)The 1 contributors listed below account for 96.1% of the provenance of Δ_{f}H° of Kr+ (g).Please note: The list is limited to 20 most important contributors or, if less, a number sufficient to account for 90% of the provenance. The Reference acts as a further link to the relevant references and notes for the measurement. The Measured Quantity is normaly given in the original units; in cases where we have reinterpreted the original measurement, the listed value may differ from that given by the authors. The quoted uncertainty is the a priori uncertainty used as input when constructing the initial Thermochemical Network, and corresponds either to the value proposed by the original authors or to our estimate; if an additional multiplier is given in parentheses immediately after the prior uncertainty, it corresponds to the factor by which the prior uncertainty needed to be multiplied during the ATcT analysis in order to make that particular measurement consistent with the prevailing knowledge contained in the Thermochemical Network.  

Influence Coefficient  TN ID  Reaction  Measured Quantity  Reference 

0.961  4131.3  Kr (g) → Kr+ (g)  Δ_{r}H°(0 K) = 112914.6 ± 0.1 cm1  Yoshino 1979 
0.038  4131.1  Kr (g) → Kr+ (g)  Δ_{r}H°(0 K) = 112914.5 ± 0.5 cm1  Moore 1970, Moore NSRDSNBS 35, Petersson 1964, est unc 
0.005  3624.1  CF4 (g) + Kr+ (g) → [CF3]+ (g) + F (g) + Kr (g)  Δ_{r}G°(300 K) = 0.24 ± 0.07 eV  Fisher 1990a 
0.000  4131.2  Kr (g) → Kr+ (g)  Δ_{r}H°(0 K) = 112925 ± 10 (×1.044) cm1  Chaghtai 1973 
0.000  4131.9  Kr (g) → Kr+ (g)  Δ_{r}H°(0 K) = 14.000 ± 0.002 eV  Kimura 1981, est unc 
0.000  4131.5  Kr (g) → Kr+ (g)  Δ_{r}H°(0 K) = 13.999 ± 0.002 eV  Nicholson 1965 
0.000  4131.8  Kr (g) → Kr+ (g)  Δ_{r}H°(0 K) = 14.01 ± 0.01 (×1.044) eV  Marquette 1985 
0.000  4131.7  Kr (g) → Kr+ (g)  Δ_{r}H°(0 K) = 14.05 ± 0.06 eV  AlJoboury 1963, est unc 
1 
B. Ruscic, R. E. Pinzon, M. L. Morton, G. von Laszewski, S. Bittner, S. G. Nijsure, K. A. Amin, M. Minkoff, and A. F. Wagner, Introduction to Active Thermochemical Tables: Several "Key" Enthalpies of Formation Revisited. J. Phys. Chem. A 108, 99799997 (2004) [DOI: 10.1021/jp047912y] 

2 
B. Ruscic, R. E. Pinzon, G. von Laszewski, D. Kodeboyina, A. Burcat, D. Leahy, D. Montoya, and A. F. Wagner, Active Thermochemical Tables: Thermochemistry for the 21^{st} Century. J. Phys. Conf. Ser. 16, 561570 (2005) [DOI: 10.1088/17426596/16/1/078] 

3 
B. Ruscic and D. H. Bross, Active Thermochemical Tables (ATcT) values based on ver. 1.122 of the Thermochemical Network (2016); available at ATcT.anl.gov 

4 
B. Ruscic, Active Thermochemical Tables: Sequential Bond Dissociation Enthalpies of Methane, Ethane, and Methanol and the Related Thermochemistry. J. Phys. Chem. A 119, 78107837 (2015) [DOI: 10.1021/acs.jpca.5b01346] 

5 
S. J. Klippenstein, L. B. Harding, and B. Ruscic, Ab initio Computations and Active Thermochemical Tables Hand in Hand: Heats of Formation of Core Combustion Species. J. Phys. Chem. A 121, 65806602 (2017) [DOI: 10.1021/acs.jpca.7b05945] 

6 
B. Ruscic, Uncertainty Quantification in Thermochemistry, Benchmarking Electronic Structure Computations, and Active Thermochemical Tables. Int. J. Quantum Chem. 114, 10971101 (2014) [DOI: 10.1002/qua.24605] 