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Items: 1 to 20 of 83

1.

Selective preparation of diamondoid phosphonates.

Fokin AA, Yurchenko RI, Tkachenko BA, Fokina NA, Gunawan MA, Poinsot D, Dahl JE, Carlson RM, Serafin M, Cattey H, Hierso JC, Schreiner PR.

J Org Chem. 2014 Jun 6;79(11):5369-73. doi: 10.1021/jo500793m. Epub 2014 May 21.

PMID:
24816428
2.

Effects of Molecular Geometry on the Properties of Compressed Diamondoid Crystals.

Yang F, Lin Y, Baldini M, Dahl JE, Carlson RM, Mao WL.

J Phys Chem Lett. 2016 Nov 17;7(22):4641-4647. Epub 2016 Nov 4.

PMID:
27801594
3.

Electronic structure tuning of diamondoids through functionalization.

Rander T, Staiger M, Richter R, Zimmermann T, Landt L, Wolter D, Dahl JE, Carlson RM, Tkachenko BA, Fokina NA, Schreiner PR, Möller T, Bostedt C.

J Chem Phys. 2013 Jan 14;138(2):024310. doi: 10.1063/1.4774268.

PMID:
23320686
4.

Altering the electronic properties of diamondoids through encapsulating small particles.

Marsusi F, Mirabbaszadeh K.

J Phys Condens Matter. 2009 May 27;21(21):215303. doi: 10.1088/0953-8984/21/21/215303. Epub 2009 May 1.

PMID:
21825546
5.

Reactivity of [1(2,3)4]pentamantane (Td-pentamantane): a nanoscale model of diamond.

Fokin AA, Schreiner PR, Fokina NA, Tkachenko BA, Hausmann H, Serafin M, Dahl JE, Liu S, Carlson RM.

J Org Chem. 2006 Oct 27;71(22):8532-40.

PMID:
17064030
6.

Functionalized nanodiamonds part I. An experimental assessment of diamantane and computational predictions for higher diamondoids.

Fokin AA, Tkachenko BA, Gunchenko PA, Gusev DV, Schreiner PR.

Chemistry. 2005 Nov 18;11(23):7091-101.

PMID:
16196063
7.

Functionalized nanodiamonds part 3: thiolation of tertiary/bridgehead alcohols.

Tkachenko BA, Fokina NA, Chernish LV, Dahl JE, Liu S, Carlson RM, Fokin AA, Schreiner PR.

Org Lett. 2006 Apr 27;8(9):1767-70.

PMID:
16623546
8.

Diamonds are a chemist's best friend: diamondoid chemistry beyond adamantane.

Schwertfeger H, Fokin AA, Schreiner PR.

Angew Chem Int Ed Engl. 2008;47(6):1022-36.

PMID:
18081112
9.

Vibrationally resolved absorption, emission and resonance Raman spectra of diamondoids: a study based on time-dependent correlation functions.

Banerjee S, Saalfrank P.

Phys Chem Chem Phys. 2014 Jan 7;16(1):144-58. doi: 10.1039/c3cp53535e.

PMID:
24226411
10.

Covalent attachment of diamondoid phosphonic acid dichlorides to tungsten oxide surfaces.

Li FH, Fabbri JD, Yurchenko RI, Mileshkin AN, Hohman JN, Yan H, Yuan H, Tran IC, Willey TM, Bagge-Hansen M, Dahl JE, Carlson RM, Fokin AA, Schreiner PR, Shen ZX, Melosh NA.

Langmuir. 2013 Aug 6;29(31):9790-7. doi: 10.1021/la401781e. Epub 2013 Jul 25.

PMID:
23855923
11.

Simple preparation of diamondoid 1,3-dienes via oxetane ring opening.

Fokin AA, Butova ED, Chernish LV, Fokina NA, Dahl JE, Carlson RM, Schreiner PR.

Org Lett. 2007 Jun 21;9(13):2541-4. Epub 2007 May 25.

PMID:
17523652
12.

Self-assembly of diamondoid molecules and derivatives (MD simulations and DFT calculations).

Xue Y, Mansoori GA.

Int J Mol Sci. 2010 Jan 21;11(1):288-303. doi: 10.3390/ijms11010288.

13.

Stable alkanes containing very long carbon-carbon bonds.

Fokin AA, Chernish LV, Gunchenko PA, Tikhonchuk EY, Hausmann H, Serafin M, Dahl JE, Carlson RM, Schreiner PR.

J Am Chem Soc. 2012 Aug 22;134(33):13641-50. doi: 10.1021/ja302258q. Epub 2012 Aug 8.

PMID:
22835264
14.

Ordered phases of encapsulated diamondoids into carbon nanotubes.

Legoas SB, dos Santos RP, Troche KS, Coluci VR, Galvão DS.

Nanotechnology. 2011 Aug 5;22(31):315708. doi: 10.1088/0957-4484/22/31/315708. Epub 2011 Jul 8.

PMID:
21737869
15.

Spatially resolved electronic and vibronic properties of single diamondoid molecules.

Wang Y, Kioupakis E, Lu X, Wegner D, Yamachika R, Dahl JE, Carlson RM, Louie SG, Crommie MF.

Nat Mater. 2008 Jan;7(1):38-42. Epub 2007 Nov 25.

PMID:
18037893
16.

Towards double-functionalized small diamondoids: selective electronic band-gap tuning.

Adhikari B, Fyta M.

Nanotechnology. 2015 Jan 21;26(3):035701. doi: 10.1088/0957-4484/26/3/035701. Epub 2014 Dec 30.

PMID:
25549002
17.

Enhanced oscillatory rectification and negative differential resistance in pentamantane diamondoid-cumulene systems.

Tawfik SA, Cui XY, Ringer SP, Stampfl C.

Nanoscale. 2016 Feb 14;8(6):3461-6. doi: 10.1039/c5nr07467c. Epub 2016 Jan 21.

PMID:
26794415
18.

Reactivities of the prism-shaped diamondoids [1(2)3]tetramantane and [12312]hexamantane (cyclohexamantane).

Fokin AA, Tkachenko BA, Fokina NA, Hausmann H, Serafin M, Dahl JE, Carlson RM, Schreiner PR.

Chemistry. 2009;15(15):3851-62. doi: 10.1002/chem.200801867.

PMID:
19229930
19.

Functionalized nanodiamonds: triamantane and [121]tetramantane.

Schreiner PR, Fokina NA, Tkachenko BA, Hausmann H, Serafin M, Dahl JE, Liu S, Carlson RM, Fokin AA.

J Org Chem. 2006 Sep 1;71(18):6709-20.

PMID:
16930019
20.

Monoprotection of diols as a key step for the selective synthesis of unequally disubstituted diamondoids (nanodiamonds).

Schwertfeger H, Würtele C, Serafin M, Hausmann H, Carlson RM, Dahl JE, Schreiner PR.

J Org Chem. 2008 Oct 3;73(19):7789-92. doi: 10.1021/jo801321s. Epub 2008 Aug 29.

PMID:
18761438

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