Bonding, Ion Mobility, and Rate-Limiting Steps in Deintercalation Reactions with ThCr₂Si₂-type KNi₂Se₂ by James R. Neilson (1896145)

“…Here, we study the nature of metal–metal bonding in the ThCr₂Si₂ structure type by probing the rate-limiting steps in the oxidative deintercalation of KNi₂Se₂. …”

Bonding, Ion Mobility, and Rate-Limiting Steps in Deintercalation Reactions with ThCr₂Si₂-type KNi₂Se₂ by James R. Neilson (1896145)

“…Here, we study the nature of metal–metal bonding in the ThCr₂Si₂ structure type by probing the rate-limiting steps in the oxidative deintercalation of KNi₂Se₂. …”

Bonding, Ion Mobility, and Rate-Limiting Steps in Deintercalation Reactions with ThCr₂Si₂-type KNi₂Se₂ by James R. Neilson (1896145)

“…Here, we study the nature of metal–metal bonding in the ThCr₂Si₂ structure type by probing the rate-limiting steps in the oxidative deintercalation of KNi₂Se₂. …”

Bonding, Ion Mobility, and Rate-Limiting Steps in Deintercalation Reactions with ThCr₂Si₂-type KNi₂Se₂ by James R. Neilson (1896145)

“…Here, we study the nature of metal–metal bonding in the ThCr₂Si₂ structure type by probing the rate-limiting steps in the oxidative deintercalation of KNi₂Se₂. …”

Effect of the stabilized MetA on the persister cell frequency under acidic conditions. by Elena A. Mordukhova (646403)

Five compounds significantly decrease MAPK1 phosphorylation in K562 cells. by Pamela Y. Ting (713174)

Effect of L-methionine on the frequency of persisters at different temperatures. by Elena A. Mordukhova (646403)

Effect of specific inhibitors on CYP-mediated CK (50 μM) metabolism in HLMs. by Jian Xiao (253329)

Growth Kinetics of Elementary Spiral Steps on Ice Prism Faces Grown in Vapor and Their Temperature Dependence by Genki Miyamoto (13914416)

Subjects:

Step length asymmetry and step width during split-belt adaptation. by Samantha Jeffcoat (22783930)

[2+2] Cycloadditions with an Iron Carbene: A Critical Step in Enyne Metathesis by Melissa R. Hoffbauer (5452868)

Assays of TUNEL revealed a decreased number of apoptotic cell after oroxylin A treatment. by Shu-Fang Lin (4167091)

Decrease in preferred walking speed with distance walked for subjects with amputation. by Nidhi Seethapathi (3258591)

The image illustrates the five steps of the experiment. by Deborah Ribeiro Frazão (9188152)

Mean and standard deviation values for the Impulse during the first 50 ms of stance (Imp50) during running shod (SH) and barefoot (BF), in both PRE and POST training, where (<sup>a... by Ana Paula da Silva Azevedo (3373688)

(a) a top view of step1 of fabrication flow, (b) cross view of Fig 2(a) along cutline A, (c) cross view of Fig 2(a) along cutline B, (d) top view of step 2 of fabrication flow, (e)... by Xiaoshi Jin (15675049)

Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

“…These contacts are characterized by the roughly parallel orientation of the inner bipyridinium ring system and the 1,2,3-triazole and 1,3-butadiyne units, as well as by the short [π···π] distances of 3.50 and 3.60 Å, respectively. …”

Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

“…These contacts are characterized by the roughly parallel orientation of the inner bipyridinium ring system and the 1,2,3-triazole and 1,3-butadiyne units, as well as by the short [π···π] distances of 3.50 and 3.60 Å, respectively. …”

Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

“…These contacts are characterized by the roughly parallel orientation of the inner bipyridinium ring system and the 1,2,3-triazole and 1,3-butadiyne units, as well as by the short [π···π] distances of 3.50 and 3.60 Å, respectively. …”

Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes by Ognjen Š. Miljanić (2485972)

“…These contacts are characterized by the roughly parallel orientation of the inner bipyridinium ring system and the 1,2,3-triazole and 1,3-butadiyne units, as well as by the short [π···π] distances of 3.50 and 3.60 Å, respectively. …”