Category:Molecular orbitals
See also category: Molecular electrical potential surfaces.method for describing the electronic structure of molecules using quantum mechanics | |||||
| Upload media | |||||
| Instance of |
| ||||
|---|---|---|---|---|---|
| |||||
 | |||||
 | This is a main category requiring frequent diffusion and maybe maintenance. As many pictures and media files as possible should be moved into appropriate subcategories. |
Subcategories
This category has the following 4 subcategories, out of 4 total.
Media in category "Molecular orbitals"
The following 200 files are in this category, out of 424 total.
(previous page) (next page)-
-
-
(PdCl4)2- MO Diagram.png 425 × 666; 94 KB
-
10 Energy to Light (2825953485).jpg 906 × 1,471; 587 KB
-
15.6 Naphthalene orbitals.svg 178 × 88; 303 KB
-
1s MO.png 312 × 177; 4 KB
-
2nd row diatomic MOs.jpg 217 × 652; 108 KB
-
2nd row diatomic MOs.png 905 × 501; 44 KB
-
2p and 3p nodes.png 1,327 × 117; 4 KB
-
2p MO.png 455 × 252; 10 KB
-
4-4photocycloadditionfmo.svg 512 × 253; 48 KB
-
4f.png 340 × 320; 58 KB
-
4fY.png 264 × 260; 31 KB
-
A(1g) - HOMO-2.png 406 × 524; 159 KB
-
A(1g)-HOMO-10.png 487 × 630; 223 KB
-
A(2g)-HOMO-3.png 496 × 547; 215 KB
-
A(2u)-HOMO-6.png 534 × 588; 246 KB
-
A1SALCs.jpg 276 × 239; 12 KB
-
-
Ag(Ar1GeGeAr1) cation.png 1,010 × 694; 42 KB
-
AH3diagram.png 2,168 × 2,742; 117 KB
-
AH3walsh2.png 1,086 × 1,386; 60 KB
-
Alkene-M Pi Backbond.png 407 × 267; 25 KB
-
Alkene-M Sigma Bond.png 426 × 275; 24 KB
-
AllylMO.png 1,186 × 1,163; 35 KB
-
Allylumlagerung Orbitale 1.svg 794 × 559; 26 KB
-
Alpha-halocarbonyls MO combination SN2.svg 334 × 96; 40 KB
-
Arg HOMOside viewArg.tif 951 × 1,469; 345 KB
-
Aromaten-Energieniveau-Schema.jpg 409 × 123; 17 KB
-
B(1g)-HOMO-11.png 470 × 636; 215 KB
-
B(1g)-LUMO.png 438 × 581; 196 KB
-
B(2g)-HOMO -1.png 382 × 496; 167 KB
-
B(2g)-HOMO-9.png 628 × 634; 294 KB
-
B(2u)-HOMO-5.png 484 × 600; 210 KB
-
B-Ar-bond-NBO-oneperspective.png 568 × 527; 79 KB
-
Bananenbindung Cyclopropan.svg 296 × 285; 14 KB
-
Bananenbindung.jpg 430 × 228; 40 KB
-
BarreleneMO representation.png 149 × 148; 2 KB
-
Benzene orbitals.png 1,030 × 822; 146 KB
-
Benzene-orbitals2.png 327 × 182; 26 KB
-
Benzylic chloride nucleophilic substitution.svg 519 × 214; 458 KB
-
Bertrand phosphinidene HOMO-LUMO.png 905 × 696; 204 KB
-
BF3 HOMO.jpg 519 × 423; 265 KB
-
BF3 LUMO.jpg 439 × 416; 250 KB
-
Bh2nh3 homo.svg 661 × 667; 2.88 MB
-
BH2NH3 orbitals.svg 512 × 517; 359 KB
-
Bindungssituation in Fischer-Carbenen.svg 856 × 726; 180 KB
-
Bolgefunksjonen psi.jpg 353 × 388; 27 KB
-
Bonding in metal carbonyls-ru.svg 439 × 184; 2 KB
-
Bonding in metal carbonyls.svg 1,180 × 500; 16 KB
-
Bonding-in-Schrock-carbenes.svg 579 × 726; 333 KB
-
Borepin HOMO-LUMO.jpg 491 × 540; 34 KB
-
Borole homolumo.png 1,024 × 1,536; 206 KB
-
Boron-trifluoride-HOMO-minus-5-Spartan-3D-balls.png 758 × 780; 255 KB
-
Buergi Dunitz Winkel.svg 463 × 523; 125 KB
-
Butadiene Ethene Cycloaddition123.png 488 × 296; 26 KB
-
Butadiene to Cyclobutadiene.png 274 × 119; 12 KB
-
Ca3Co2O6 press.png 2,604 × 1,521; 578 KB
-
Calculated HOMO of (P(NH2)2)+.png 492 × 384; 24 KB
-
Calculated HOMO of (PF2)+.png 492 × 384; 36 KB
-
Calculated HOMO-1 of (P(NH2)2)+.png 492 × 384; 21 KB
-
Calculated LUMO of (P(NH2)2)+.png 492 × 384; 30 KB
-
Calculated LUMO of (PF2)+.png 492 × 384; 28 KB
-
CAMY-B3LYP frontier MOs of dianions.png 1,202 × 1,548; 827 KB
-
Carbene alkene orbitals.png 957 × 622; 19 KB
-
Carbon dioxide antibonding orbital.png 510 × 348; 71 KB
-
Carbon dioxide molecular orbital.png 481 × 303; 72 KB
-
Carbon Dioxide Molecular Orbitals.png 1,030 × 1,004; 142 KB
-
Carbon-monoxide-HOMO-phase-3D-balls.png 1,100 × 863; 245 KB
-
Carbon-monoxide-HOMO-phase-3D-balls.svg 752 × 572; 15 KB
-
Carbon-monoxide-LUMO-phase-3D-balls.png 1,000 × 1,100; 345 KB
-
Cartoon localized molecular orbitals.png 3,002 × 1,513; 84 KB
-
CBC scheme.png 687 × 344; 36 KB
-
CF Diagram TH.png 3,253 × 1,241; 80 KB
-
CFT分裂.jpg 949 × 1,050; 189 KB
-
Chem507f09sqvstet.png 464 × 488; 5 KB
-
Cinnamaldehyde-3D-pi-MO.png 1,068 × 564; 106 KB
-
Clorobenzene orbitali.jpg 399 × 132; 32 KB
-
CO2 HOMO 3D.png 406 × 329; 60 KB
-
CO2 LUMO translucent mix.png 4,009 × 3,576; 749 KB
-
CO2 LUMO.gif 424 × 321; 7.37 MB
-
Co2lumo.png 469 × 356; 47 KB
-
Construction of frontier orbitals.tiff 1,748 × 301; 19 KB
-
Contour-surfaces-of-frontier-molecular-orbitals-of-O-Anisic-acid.jpg 600 × 662; 130 KB
-
COT rad anion Frost orbs.png 939 × 603; 15 KB
-
Covalent&PolarBond.png 1,128 × 600; 17 KB
-
CovalentBond.png 1,128 × 600; 17 KB
-
Cyclobutadiene (2minus) with MO diagram.png 180 × 200; 604 bytes
-
Cyclobutadiene (2plus) with MO diagram.png 180 × 200; 481 bytes
-
Cyclobutadiene antiaromaticity.jpg 1,062 × 1,037; 151 KB
-
Cyclobutadiene with MO diagram.png 180 × 200; 411 bytes
-
Cyclobutene Electrocyclic Ring Opening.png 497 × 144; 18 KB
-
Cyclobutene ring opening.jpg 497 × 144; 11 KB
-
Cycloheptatriene (1minus) with MO diagram.png 180 × 200; 844 bytes
-
Cycloheptatriene (1plus) with MO diagram.png 180 × 200; 800 bytes
-
Cyclohexa13diene opt HOMO.png 1,380 × 1,338; 249 KB
-
Cyclohexa13diene opt LUMO.png 1,380 × 1,338; 253 KB
-
Cyclopentadiene (1minus) with MO diagram.png 180 × 200; 767 bytes
-
Cyclopentadiene (1plus) with MO diagram.png 180 × 200; 718 bytes
-
Cyclopentadiene Maleic Anhydride Diels Alder.png 449 × 395; 44 KB
-
Cyclopropene (1minus) with MO diagram.png 180 × 200; 998 bytes
-
Cyclopropene (1plus) with MO diagram.png 180 × 200; 954 bytes
-
Cyclopropene radical with MO diagram.png 180 × 200; 872 bytes
-
D-d-delta-MO-solid-3D-balls.png 1,100 × 780; 202 KB
-
D-d-delta-MO-transparent-3D-balls.png 1,100 × 780; 331 KB
-
D-d-pi-MO-solid-3D-balls.png 1,100 × 715; 182 KB
-
D-d-pi-MO-transparent-3D-balls.png 1,100 × 751; 343 KB
-
D1-octahedral-crystal-field.png 1,656 × 581; 15 KB
-
D5cfse.png 377 × 147; 9 KB
-
D6cfse.png 376 × 147; 9 KB
-
DA1 ts opt am1 HOMO.png 1,599 × 1,338; 286 KB
-
DA1 ts opt am1 LUMO.png 1,599 × 1,338; 286 KB
-
Dative covalent bond.png 480 × 426; 35 KB
-
Dative covalent bond2.png 480 × 426; 97 KB
-
DCD-Model-MO-diagram-part-1.svg 475 × 544; 293 KB
-
DCD-Model-MO-diagram-part-2.svg 475 × 544; 221 KB
-
DCD-Modell-Metallacyclopropan-MO-diagram.svg 512 × 355; 58 KB
-
Delta-bond-formation-2D.png 1,100 × 300; 61 KB
-
Desdoblamiento de orbitales .jpg 1,240 × 1,754; 61 KB
-
Dewar Benzene Frontier Orbitals.png 1,762 × 643; 24 KB
-
DFT optimised frontier molecular orbitals of corroles.png 692 × 1,080; 205 KB
-
-
Diagrama alto spin.png 385 × 155; 4 KB
-
Diagrama bajo spin.PNG 364 × 165; 4 KB
-
Diagrama orbital Carbono.svg 1,392 × 1,471; 45 KB
-
Diatomic MO1.jpg 3,500 × 2,683; 816 KB
-
Diatomic MO2.jpg 3,496 × 2,679; 809 KB
-
Diazaborole.png 2,400 × 768; 219 KB
-
Diels-Alder cyclopentadiene maleic anhydride.svg 392 × 227; 117 KB
-
Dihapnik.png 424 × 924; 110 KB
-
Dilämmastik.png 391 × 917; 93 KB
-
Dimolybdenum-Mo2-delta-bond-Spartan-HF-3-21G-3D-end.png 720 × 721; 261 KB
-
Dimolybdenum-Mo2-delta-bond-Spartan-HF-3-21G-3D-side.png 862 × 759; 301 KB
-
Disrotatory electrophilic reaction molecular orbitals.svg 369 × 372; 182 KB
-
Disüsinik.png 445 × 914; 93 KB
-
E(g)-HOMO-7.png 1,160 × 548; 412 KB
-
E(g)-HOMO.png 912 × 586; 376 KB
-
E(u)-HOMO-4.png 1,123 × 459; 309 KB
-
E(u)-HOMO-8.png 1,268 × 485; 417 KB
-
Electron Density Repulsion.png 975 × 356; 43 KB
-
ElectronDensityAniline.PNG 420 × 486; 52 KB
-
Electrostatic potential map benzyne.jpg 201 × 119; 10 KB
-
Empty mixing orbitals.png 433 × 437; 9 KB
-
Endo da am1 HOMO.png 1,746 × 1,338; 276 KB
-
Endo da am1 LUMO.png 1,746 × 1,338; 335 KB
-
Energy gap and electron hopping.png 456 × 215; 14 KB
-
Enolate-pi-MOs.png 2,200 × 1,914; 805 KB
-
ES1 of butadiene.png 893 × 1,094; 116 KB
-
Exo da opt am1 HOMO.png 1,464 × 1,338; 257 KB
-
Exo da opt am1 LUMO.png 1,464 × 1,338; 275 KB
-
Fe2S2(CO)6 LUMO.png 423 × 426; 134 KB
-
Ficuria3.png 642 × 234; 5 KB
-
Figangorb.png 454 × 238; 22 KB
-
Figefeitoindutivo.png 608 × 414; 11 KB
-
Figefeitomesomerico.png 892 × 350; 12 KB
-
Figestruturas.png 493 × 178; 29 KB
-
Figura1.JPG 478 × 140; 13 KB
-
Figure 2 Relative Energies of Pi orbitals.png 957 × 219; 42 KB
-
Figure one (Sigma donation).png 342 × 594; 20 KB
-
FMO control of regiochemistry.svg 512 × 259; 28 KB
-
FMO method sigmatropic rearrangements.svg 480 × 253; 98 KB
-
FMO of Diels-Alder reaction.png 1,670 × 1,541; 50 KB
-
Formaldehyde Molecular Orbitals.jpg 494 × 652; 228 KB
-
Formaldehyde-LUMO-transparent-3D-balls.png 1,084 × 1,100; 392 KB
-
Formamide-MO-3D-balls.png 990 × 1,100; 240 KB
-
Formação da ligação suprafacial e antarafacial.png 410 × 306; 19 KB
-
Frontier MO Diagram of Planar and Bent ferrocenylmethylium.png 1,059 × 1,222; 80 KB
-
Frontier molecular orbitals overlap in 1,3-dipolar cycloadditions.tif 1,304 × 559; 60 KB
-
Frontier orbital energies (in eV) of porphyrin molecule.png 664 × 354; 213 KB
-
Frontier orbital energies (in eV) of the pyrrole monomers.png 657 × 497; 257 KB
-
Frontier orbitals of alkyl-substituted trisilaallene.png 1,624 × 833; 349 KB
-
Frontier orbitals of silyl-substituted trisilaallene.png 1,724 × 972; 327 KB
-
Frost MH.gif 687 × 311; 13 KB
-
Frost-MH.gif 687 × 311; 12 KB
-
Gebor.png 2,346 × 1,216; 415 KB
-
General D4h Molecular Orbital .jpg 3,024 × 2,571; 1.87 MB
-
Generic D4h MO Diagram.png 605 × 665; 98 KB
-
Gouterman’s historic diagram of porphyrin MOs.png 470 × 551; 86 KB
-
H2O2 EHM Orb-5.jpg 262 × 256; 23 KB
-
H3 walsh diagram.jpg 3,396 × 1,819; 714 KB
-
H4 MO diagram.png 1,892 × 1,392; 106 KB
-
Happimolekyylin molekyyliorbitaalidiagrammi.svg 756 × 831; 47 KB
-
HCl mo diagram.png 1,676 × 956; 14 KB
-
HCl MO energy diagram.png 1,618 × 742; 14 KB
-
HClmodiagram.png 1,676 × 956; 14 KB
-
He2 antibonding orbital.png 294 × 256; 7 KB
-
He2 antibonding orbital.svg 600 × 522; 2 KB
-
Hibridación de orbitales 2s y 2p para formar el sp2.svg 512 × 362; 48 KB
-
Hibridación sp.svg 3,926 × 1,310; 472 KB
-
Hibridación sp^3 de un átomo de carbono.svg 512 × 362; 39 KB
-
High-low-spin-Co2+.png 875 × 1,146; 24 KB
-
Hin- und Rückbindung, DCD Modell.svg 145 × 46; 304 KB
-
HOMO and LUMO Orbitals for AlCl.png 512 × 384; 27 KB
-
HOMO LUMO.png 480 × 289; 6 KB
-
Homo lumo.png 512 × 424; 50 KB
-
HOMO of (PH2)+.png 492 × 384; 29 KB
-
Homo-lumo gap.tif 1,254 × 1,238; 232 KB
-
HOMO-LUMO orbitals in phoshpaallenes.png 340 × 182; 49 KB
-
HOMOLUMObenzilicRearrangement.png 455 × 228; 4 KB
-
Hopping mechanism.PNG 533 × 292; 44 KB
_Valence_orbital_diagram_showing_the_donation_of_a_lone_pair_on_heteroatom_E_to_the_vacant_6p_orbital_of_adjacent_Pb.png){kind=small}
6)Cl3_eta_(Cr(NH3)6)Cl3_konposatuen_arteko_kolore_diferentzia.png)
2-_MO_Diagram.png)
.jpg)
_-_HOMO-2.png)
-HOMO-10.png)
-HOMO-3.png)
-HOMO-6.png)
_cation.png)
-HOMO-11.png)
-LUMO.png)
-HOMO_-1.png)
-HOMO-9.png)
-HOMO-5.png)
2)%2B.png)
%2B.png)
2)%2B.png)
2)%2B.png)
%2B.png)
_with_MO_diagram.png)
_with_MO_diagram.png)
_with_MO_diagram.png)
_with_MO_diagram.png)
_with_MO_diagram.png)
_with_MO_diagram.png)
_with_MO_diagram.png)
_with_MO_diagram.png)
-HOMO-7.png)
-HOMO.png)
-HOMO-4.png){kind=small}
-HOMO-8.png){kind=small}
6_LUMO.png)
.png)
_of_porphyrin_molecule.png)
_of_the_pyrrole_monomers.png)
%2B.png)
