Erratum to The effect of molecular polarity on nem/catic phase stability in 12-vertex carboranes (Liquid Crystals, 2014, 41, 8, (1188-1198), 10.1080/02678292.2014.911371);The effect of molecular polarity on nem/catic phase stability in 12-vertex carboranes

Liquid Crystals

Volumn 41, Issue 8, 2014, Pages 1188-1198

  Pecyna, Jacek ^a   Denicola, Richard P ^a   Gray, Harrison M ^a   Ringstrand, Bryan ^a   Kaszynski, Piotr ^a,b  

^a VANDERBILT UNIVERSITY   (United States)

^b UNIVERSITY OF LODZ   (Poland)

Author keywords

carboranes; DFT calculations; nematic; phase stability; polarity; synthesis

Indexed keywords

EID: 84901588156     PISSN: 02678292     EISSN: 13665855     Source Type: Journal    
DOI: 10.1080/02678292.2014.949607     Document Type: Erratum

References (27)

1. Kirsch P, Bremer M. Nematic liquid crystals for active matrix displays: molecular design and synthesis. Angew Chem Int Ed. 2000;39:4216-4235. doi:10.1002/1521-3773(20001201)39:23<4216::AID-ANIE4216>3.0.CO;2-K
2. Bremer M, Lietzau L. 1,1,6,7-tetrafluoroindanes: improved liquid crystals for LCD-TV application. New J Chem. 2005;29:72-74. doi:10.1039/b414312d
3. Blinov LM. Behavior of liquid crystals in electric and magnetic fields. In: Demus D, Goodby J, Gray GW, Spiess H-W, Vill V, editors. Hadbook of liquid crystals. Vol. 1. New York (NY): Willey-VCH; 1998. p. 477-534.
4. Blinov LM, Chigrinov VG. Electrooptic effects in liquid crystal materials. New York (NY): Springer-Verlag; 1994.
5. Kaszynski P, Pakhomov S, Gurskii ME, Erdyakov SY, Starikova ZA, Lyssenko KA, Antipin MY, Young VG Jr, Bubnov YN. 1-pyridine- and 1-quinuclidine-1-boraadamantane as models for derivatives of 1-borabicyclo[2.2.2]octane. Experimental and theoretical evaluation of the B-N fragment as a polar isosteric substitution for the C-C group in liquid crystal compounds. J Org Chem. 2009;74:1709-1720. doi:10.1021/jo802504c
6. 10 ]. J Mater Chem. 2010;20:9613-9615. doi:10.1039/c0jm02876b
7. - cluster. J Mater Chem. 2011;21:90-95. doi:10.1039/c0jm02075c
8. - anion. Inorg Chem. 2011;50:2654-2660. doi:10.1021/ic102557s
9. - cluster. (submitted).
10. - clusters. J Mater Chem. 2012;22:4874-4880. doi:10.1039/c2jm15448j
11. 2 ] as key precursors to advanced materials: synthesis and reactivity. Inorg Chem. 2010;49:1166-1179. doi:10.1021/ic9021323
12. - under similar conditions in a microwave oven was recently reported: Konieczka SZ, Himmelspach A, Hailmann M, Finze M. Synthesis, characterization, and selected properties of 7- and 12-ammoniocarba-closo-dodecaboranes. Eur J Inorg Chem. 2013;134-146. doi:10.1002/ejic.201200969
13. Ohta K, Januszko A, Kaszynski P, Nagamine T, Sasnouski G, Endo Y. Structural effects in three-ring mesogenic derivatives of p-carborane and their hydrocarbon analogues. Liq Cryst. 2004;31:671-682. doi:10.1080/02678290410001670584
14. Endo Y, Iijima T, Yamakoshi Y, Fukasawa H, Miyaura C, Inada M, Kubo A, Itai A. Potent estrogen agonists based on carborane as a hydrophobic skeletal structure: a new medicinal application of boron clusters. Chem Biol. 2001;8:341-355. doi:10.1016/S1074-5521(01)00016-3
15. Douglass AG, Pakhomov S, Reeves B, Janoušek Z, Kaszynski P. Triphenylsilyl as a protecting group in the synthesis of 1,12-heterodisubstituted p-carboranes. J Org Chem. 2000;65:1434-1441. doi:10.1021/jo991588z
16. Zhao Y, Truhlar DG. The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals. Theor Chem Acc. 2008;120:215-241.
17. Chan T-N, Lu Z, Yam W-S, Yeap G-Y, Imrie CT. Non-symmetric liquid crystal dimers containing an isoflavone moiety. Liq Cryst. 2012;39:393-402. doi:10.1080/02678292.2012.658712
18. Kaszynski P, Januszko A, Ohta K, Nagamine T, Potaczek P, Young VG Jr, Endo Y. Conformational effects on mesophase stability: numerical comparison of carborane diester homologous series with their bicyclo[2.2.2]octane, cyclohexane and benzene analogues. Liq Cryst. 2008;35:1169-1190. doi:10.1080/02678290802409775
19. Kaszynski P. Closo-boranes as structural elements for liquid crystals. In: Hosmane N, editor. Boron science: new technologies & applications. New York (NY): CRC Press; 2012. p. 305-338.
20. Gavrilovic DM. United States patent US 3.925.238. 1975; Liqcrys 5.0 database, compound #25521.
21. Januszko A, Glab KL, Kaszynski P, Patel K, Lewis RA, Mehl GH, Wand MD. The effect of carborane, bicyclo[2.2.2]octane and benzene on mesogenic and dielectric properties of laterally fluorinated three-ring mesogens. J Mater Chem. 2006;16:3183-3192. doi:10.1039/b600068a
22. Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Scuseria GE, Robb MA, Cheeseman JR, Scalmani G, Barone V, Mennucci B, Petersson GA, Nakatsuji H, Caricato M, Li X, Hratchian HP, Izmaylov AF, Bloino J, Zheng G, Sonnenberg JL, Hada M, Ehara M, Toyota K, Fukuda R, Hasegawa J, Ishida M, Nakajima T, Honda Y, Kitao O, Nakai H, Vreven T, Montgomery Jr JA, Peralta JE, Ogliaro F, Bearpark M, Heyd JJ, Brothers E, Kudin KN, Staroverov VN, Kobayashi R, Normand J, Raghavachari K, Rendell A, Burant JC, Iyengar SS, Tomasi J, Cossi M, Rega N, Millam JM, Klene M, Knox JE, Cross JB, Bakken V, Adamo C, Jaramillo J, Gomperts R, Stratmann RE, Yazyev O, Austin AJ, Cammi R, Pomelli C, Ochterski JW, Martin RL, Morokuma K, Zakrzewski VG, Voth GA, Salvador P, Dannenberg JJ, Dapprich S, Daniels AD, Farkas O, Foresman JB, Ortiz JV, Cioslowski J, Fox DJ. Gaussian 09, revision A.02. Wallingford (CT): Gaussian; 2009.
23. Simon S, Duran M, Dannenberg JJ. How does basis set superposition error change the potential surfaces for hydrogen-bonded dimers? J Chem Phys. 1996;105:11024-11031. doi:10.1063/1.472902
24. Cossi M, Scalmani G, Rega N, Barone V. New developments in the polarizable continuum model for quantum mechanical and classical calculations on molecules in solution. J Chem Phys. 2002;117:43-54 and references therein. doi:10.1063/1.1480445
25. - anion for liquid crystal display applications. J Mater Chem C. 2014;2:2956-2964. doi:10.1039/c4tc00230j
26. Kaszynski P, Huang J, Jenkins GS, Bairamov KA, Lipiak D. Boron clusters in liquid crystals. Mol Cryst Liq Cryst. 1995;260:315-332. doi:10.1080/10587259508038705
27. Burns DH, Miller JD, Chan H-K, Delaney MO. Scope and utility of a new soluble copper catalyst [CuBr-LiSPh-LiBr-THF]: a comparison with other copper catalysts in their ability to couple one equivalent of a grignard reagent with an alkyl sulfonate. J Am Chem Soc. 1997;119:2125-2133. doi:10.1021/ja963944q