14,051 Works

Data from: A supermatrix phylogeny of corvoid passerine birds (Aves: Corvides)

Knud Andreas Jønsson, Pierre-Henri Fabre, Jonathan D. Kennedy, Ben G. Holt, Michael K. Borregaard, Carsten Rahbek & Jon Fjeldså
The Corvides (previously referred to as the core Corvoidea) are a morphologically diverse clade of passerine birds comprising nearly 800 species. The group originated some 30 million years ago in the proto-Papuan archipelago, to the north of Australia, from where lineages have dispersed and colonized all of the world’s major continental and insular landmasses (except Antarctica). During the last decade multiple species-level phylogenies have been generated for individual corvoid families and more recently the inter-familial...

Streptorubin atropisomer

Henry Rzepa
(S)-Streptorubin dimer, calculated optical rotation

Data from: Sex drives intra-cellular conflict in yeast

Ellie Harrison, R. Craig MacLean, Vassiliki Koufopanou, Austin Burt, R. C. MacLean, V. Koufopanou & A. Burt
Theory predicts that sex can drive the evolution of conflict within the cell. During asexual reproduction genetic material within the cell is inherited as a single unit, selecting for cooperation both within the genome as well as between the extra-genomic elements within the cell (e.g. plasmids and endosymbionts). Under sexual reproduction this unity is broken down as parental genomes are distributed between meiotic progeny. Genetic elements able to transmit to more than 50% of meiotic...

Data from: Evolution of displays within the pair bond

Maria R. Servedio, Trevor D. Price, Russell Lande, R. Lande, T. D. Price & M. R. Servedio
Although sexual selection is an important cause of display evolution, in socially monogamous species (e.g. many birds), displays continue after formation of the pair bond. Here, we consider that these displays evolve because they stimulate the partner to increase investment in offspring. Our study is motivated by elaborate mutual displays in species that are largely monomorphic and have long-term pair bonds (e.g. the great crested grebe, Podiceps cristatus) and by many empirical results evidencing that...

Se(SiH3)6 Wiberg

Henry Rzepa
Gaussian Calculation

SeMe2(SiH3)4 Wiberg

Henry Rzepa
Gaussian Calculation

Cr4 anti-aromaticity, singlet freq

Henry Rzepa
Gaussian Calculation

Cr4 aromaticity? singlet

Henry Rzepa
Gaussian Calculation

(t-butyl)3PF2 TS for F2 elimination

Henry Rzepa
Gaussian Calculation

p-Cl phenylboroxine + 3H2O alt H-bond in 3H2O, C3

Henry Rzepa
Gaussian Calculation

Compound 2b

Clare Bakewell
NMR data

Compd6_300K_C6D6

Henry Rzepa
Bruker and MestreNova NMR Datasets

CO (2+) CASSCF(12,12)

Henry Rzepa
Gaussian Calculation

11B. COQFOE

Henry Rzepa
Gaussian Calculation

3, TPSSh/3-21G*/SCRF=chloroform, IRC for Fe-Fe bond shift

Henry Rzepa
Gaussian 16 Calculation

B2 Excited singlet exhibiting triple BB bond.

Henry Rzepa
Gaussian Calculation

(Z) H TS 4 (freq)

Bethan Coulson
Gaussian Calculation

Rb2 (2-) triplet

Henry Rzepa
Gaussian Calculation

I. I7, D5h, Def2-QZVPPD, B3LYP

Henry Rzepa
Gaussian Calculation

I.I1, Def2-QZVPPD

Henry Rzepa
Gaussian Calculation

TS1 PT -1006.494613 (+14.9) 10.14469/hpc/3190 IRC: 10.14469/hpc/3192

Henry Rzepa
Gaussian Calculation

Lidocaine HCl + H2O, ionic form

Henry Rzepa
Gaussian Calculation

Cr4 Me8 YQC convergence, quintet, C2h, TPSSh

Henry Rzepa
Gaussian Calculation

Cr4 Me8 YQC convergence, di-cation, singlet

Henry Rzepa
Gaussian Calculation

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