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Phylogeny and biogeography in Solanaceae, Verbenaceae and Bignoniaceae: a comparison of continental and intercontinental diversification patterns

STEM and diversification

Olmstead RG.
GSID: fOXHPLCS3boJ
RG Olmstead - Botanical Journal of the Linnean Society, 2013 - academic.oup.com

… Estimated dates for the stem lineages of all three families imply origins in the Late … contribute to a better understanding of the in situ diversification of the South American flora. …

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Olmstead, R. G. (2013). Phylogeny and biogeography in Solanaceae, Verbenaceae and Bignoniaceae: a comparison of continental and intercontinental diversification patterns. Botanical Journal of the Linnean Society, 171(1), 80-102.
Olmstead, Richard G. "Phylogeny and biogeography in Solanaceae, Verbenaceae and Bignoniaceae: a comparison of continental and intercontinental diversification patterns." Botanical Journal of the Linnean Society 171.1 (2013): 80-102.
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Silver(I)-Mediated Modification, Dimerization, and Polymerization of an Open-Cage Fullerene.

Journal of the American Chemical Society

Aghabali A, Jun S, Olmstead MM, Balch AL.
PMID: 27936651
J Am Chem Soc. 2016 Dec 21;138(50):16459-16465. doi: 10.1021/jacs.6b10394. Epub 2016 Dec 12.

The reactions of the open-cage fullerene, MMK-9, with an open 12-membered ring on its surface and silver(I) salts have been examined. The structure of MMK-9 itself has been determined by single-crystal X-ray diffraction. MMK-9 reacts with silver trifluoroacetate in...

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Aghabali A, Jun S, Olmstead MM, et al. Silver(I)-Mediated Modification, Dimerization, and Polymerization of an Open-Cage Fullerene. J Am Chem Soc. 2016;138(50):16459-16465doi: 10.1021/jacs.6b10394.
Aghabali, A., Jun, S., Olmstead, M. M., & Balch, A. L. (2016). Silver(I)-Mediated Modification, Dimerization, and Polymerization of an Open-Cage Fullerene. Journal of the American Chemical Society, 138(50), 16459-16465. https://doi.org/10.1021/jacs.6b10394
Aghabali, Amineh, et al. "Silver(I)-Mediated Modification, Dimerization, and Polymerization of an Open-Cage Fullerene." Journal of the American Chemical Society vol. 138,50 (2016): 16459-16465. doi: https://doi.org/10.1021/jacs.6b10394
Aghabali A, Jun S, Olmstead MM, Balch AL. Silver(I)-Mediated Modification, Dimerization, and Polymerization of an Open-Cage Fullerene. J Am Chem Soc. 2016 Dec 21;138(50):16459-16465. doi: 10.1021/jacs.6b10394. Epub 2016 Dec 12. PMID: 27936651.
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Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride.

Chemical communications (Cambridge, England)

Erickson JD, Lai TY, Liptrot DJ, Olmstead MM, Power PP.
PMID: 27711364
Chem Commun (Camb). 2016 Nov 17;52(94):13656-13659. doi: 10.1039/c6cc06963k.

The facile heterodehydrocoupling of a range of primary or secondary amines and even ammonia with pinacolborane (HBPin) was accomplished using {Ar

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Erickson JD, Lai TY, Liptrot DJ, et al. Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride. Chem Commun (Camb). 2016;52(94):13656-13659doi: 10.1039/c6cc06963k.
Erickson, J. D., Lai, T. Y., Liptrot, D. J., Olmstead, M. M., & Power, P. P. (2016). Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride. Chemical communications (Cambridge, England), 52(94), 13656-13659. https://doi.org/10.1039/c6cc06963k
Erickson, Jeremy D, et al. "Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride." Chemical communications (Cambridge, England) vol. 52,94 (2016): 13656-13659. doi: https://doi.org/10.1039/c6cc06963k
Erickson JD, Lai TY, Liptrot DJ, Olmstead MM, Power PP. Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride. Chem Commun (Camb). 2016 Nov 17;52(94):13656-13659. doi: 10.1039/c6cc06963k. PMID: 27711364.
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Synthesis, Structure, and Properties of {N,N'- Bis[2-(2-pyridyl)ethyl]pyridine-2,6-dicarboxamido}copper(II).

Inorganic chemistry

Chavez FA, Olmstead MM, Mascharak PK.
PMID: 11666346
Inorg Chem. 1996 Feb 28;35(5):1410-1412. doi: 10.1021/ic9512136.

No abstract available.

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Chavez FA, Olmstead MM, Mascharak PK. Synthesis, Structure, and Properties of {N,N'- Bis[2-(2-pyridyl)ethyl]pyridine-2,6-dicarboxamido}copper(II). Inorg Chem. 1996;35(5):1410-1412doi: 10.1021/ic9512136.
Chavez, F. A., Olmstead, M. M., & Mascharak, P. K. (1996). Synthesis, Structure, and Properties of {N,N'- Bis[2-(2-pyridyl)ethyl]pyridine-2,6-dicarboxamido}copper(II). Inorganic chemistry, 35(5), 1410-1412. https://doi.org/10.1021/ic9512136
Chavez, Ferman A., et al. "Synthesis, Structure, and Properties of {N,N'- Bis[2-(2-pyridyl)ethyl]pyridine-2,6-dicarboxamido}copper(II)." Inorganic chemistry vol. 35,5 (1996): 1410-1412. doi: https://doi.org/10.1021/ic9512136
Chavez FA, Olmstead MM, Mascharak PK. Synthesis, Structure, and Properties of {N,N'- Bis[2-(2-pyridyl)ethyl]pyridine-2,6-dicarboxamido}copper(II). Inorg Chem. 1996 Feb 28;35(5):1410-1412. doi: 10.1021/ic9512136. PMID: 11666346.
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Structural and Spectroscopic Characterization of Iron(III) Dioxoporphodimethene Complexes and Their Autoreduction to an Iron(II) Complex in Pyridine.

Inorganic chemistry

Balch AL, Noll BC, Olmstead MM, Phillips SL.
PMID: 11666797
Inorg Chem. 1996 Oct 23;35(22):6495-6506. doi: 10.1021/ic960423v.

Three iron complexes of the meso-dioxo derivative of octaethylporphryin (trans-H(2)OEPO(2)) were characterized by X-ray diffraction. Green ClFe(III)(trans-OEPO(2)).1.5C(6)H(6) crystallizes in the monoclinic space group P2(1)/c with a = 13.766(3) Å, b = 19.075(3) Å, c = 15.217(3) Å, beta =...

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Balch AL, Noll BC, Olmstead MM, et al. Structural and Spectroscopic Characterization of Iron(III) Dioxoporphodimethene Complexes and Their Autoreduction to an Iron(II) Complex in Pyridine. Inorg Chem. 1996;35(22):6495-6506doi: 10.1021/ic960423v.
Balch, A. L., Noll, B. C., Olmstead, M. M., & Phillips, S. L. (1996). Structural and Spectroscopic Characterization of Iron(III) Dioxoporphodimethene Complexes and Their Autoreduction to an Iron(II) Complex in Pyridine. Inorganic chemistry, 35(22), 6495-6506. https://doi.org/10.1021/ic960423v
Balch, Alan L., et al. "Structural and Spectroscopic Characterization of Iron(III) Dioxoporphodimethene Complexes and Their Autoreduction to an Iron(II) Complex in Pyridine." Inorganic chemistry vol. 35,22 (1996): 6495-6506. doi: https://doi.org/10.1021/ic960423v
Balch AL, Noll BC, Olmstead MM, Phillips SL. Structural and Spectroscopic Characterization of Iron(III) Dioxoporphodimethene Complexes and Their Autoreduction to an Iron(II) Complex in Pyridine. Inorg Chem. 1996 Oct 23;35(22):6495-6506. doi: 10.1021/ic960423v. PMID: 11666797.
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Isomeric forms of divalent heavier group 14 element hydrides: characterization of Ar'(H)GeGe(H)Ar' and Ar'(H)(2)GeGeAr'.PMe(3) (Ar' = C(6)H(3)-2,6-Dipp(2); Dipp = C(6)H(3)-2,6-Pr(i)(2)).

Journal of the American Chemical Society

Richards AF, Phillips AD, Olmstead MM, Power PP.
PMID: 12630862
J Am Chem Soc. 2003 Mar 19;125(11):3204-5. doi: 10.1021/ja029772g.

The reduction of Ar'GeCl (Ar' = C6H3-2,6-Dipp2; Dipp = C6H3-2,6-Pri2) with LiBH(Bus)3 affords the first heavier group 14 element dimetallene hydride Ar'(H)GeGe(H)Ar' which, upon further reaction with PMe3, yields the base-stabilized isomeric form Ar'(H)2GeGeAr'.PMe3.

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Richards AF, Phillips AD, Olmstead MM, et al. Isomeric forms of divalent heavier group 14 element hydrides: characterization of Ar'(H)GeGe(H)Ar' and Ar'(H)(2)GeGeAr'.PMe(3) (Ar' = C(6)H(3)-2,6-Dipp(2); Dipp = C(6)H(3)-2,6-Pr(i)(2)). J Am Chem Soc. 2003;125(11):3204-5doi: 10.1021/ja029772g.
Richards, A. F., Phillips, A. D., Olmstead, M. M., & Power, P. P. (2003). Isomeric forms of divalent heavier group 14 element hydrides: characterization of Ar'(H)GeGe(H)Ar' and Ar'(H)(2)GeGeAr'.PMe(3) (Ar' = C(6)H(3)-2,6-Dipp(2); Dipp = C(6)H(3)-2,6-Pr(i)(2)). Journal of the American Chemical Society, 125(11), 3204-5. https://doi.org/10.1021/ja029772g
Richards, Anne F, et al. "Isomeric forms of divalent heavier group 14 element hydrides: characterization of Ar'(H)GeGe(H)Ar' and Ar'(H)(2)GeGeAr'.PMe(3) (Ar' = C(6)H(3)-2,6-Dipp(2); Dipp = C(6)H(3)-2,6-Pr(i)(2))." Journal of the American Chemical Society vol. 125,11 (2003): 3204-5. doi: https://doi.org/10.1021/ja029772g
Richards AF, Phillips AD, Olmstead MM, Power PP. Isomeric forms of divalent heavier group 14 element hydrides: characterization of Ar'(H)GeGe(H)Ar' and Ar'(H)(2)GeGeAr'.PMe(3) (Ar' = C(6)H(3)-2,6-Dipp(2); Dipp = C(6)H(3)-2,6-Pr(i)(2)). J Am Chem Soc. 2003 Mar 19;125(11):3204-5. doi: 10.1021/ja029772g. PMID: 12630862.
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Crystallographic characterization of isomer 2 of Er2@C82 and comparison with isomer 1 of Er2@C82.

Chemical communications (Cambridge, England)

Olmstead MM, Lee HM, Stevenson S, Dorn HC, Balch AL.
PMID: 12510300
Chem Commun (Camb). 2002 Nov 21;(22):2688-9. doi: 10.1039/b209270k.

The X-ray crystal structure of (Isomer 2 of Er2@C82). NiII(OEP).2(benzene) shows that the fullerene cage in Isomer 2 of Er2@C82 is the C3v isomer (82:8) and that the erbium ions are distributed over 23 interior sites with occupancies ranging...

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Olmstead MM, Lee HM, Stevenson S, et al. Crystallographic characterization of isomer 2 of Er2@C82 and comparison with isomer 1 of Er2@C82. Chem Commun (Camb). 2002;(22):2688-9doi: 10.1039/b209270k.
Olmstead, M. M., Lee, H. M., Stevenson, S., Dorn, H. C., & Balch, A. L. (2002). Crystallographic characterization of isomer 2 of Er2@C82 and comparison with isomer 1 of Er2@C82. Chemical communications (Cambridge, England), (22), 2688-9. https://doi.org/10.1039/b209270k
Olmstead, Marilyn M, et al. "Crystallographic characterization of isomer 2 of Er2@C82 and comparison with isomer 1 of Er2@C82." Chemical communications (Cambridge, England) vol. ,22 (2002): 2688-9. doi: https://doi.org/10.1039/b209270k
Olmstead MM, Lee HM, Stevenson S, Dorn HC, Balch AL. Crystallographic characterization of isomer 2 of Er2@C82 and comparison with isomer 1 of Er2@C82. Chem Commun (Camb). 2002 Nov 21;(22):2688-9. doi: 10.1039/b209270k. PMID: 12510300.
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Synthesis and characterization of three-coordinate and related beta-diketiminate derivatives of manganese, iron, and cobalt.

Inorganic chemistry

Panda A, Stender M, Wright RJ, Olmstead MM, Klavins P, Power PP.
PMID: 12132915
Inorg Chem. 2002 Jul 29;41(15):3909-16. doi: 10.1021/ic025552s.

Treatment of M[N(SiMe(3))(2)](2) (M = Mn, Fe, Co) with various bulky beta-diketimines afforded a variety of new three-coordinate complexes which were characterized by UV-vis, (1)H NMR and IR spectroscopy, magnetic measurements, and X-ray crystallography. Reaction of the beta-diketimine H(Dipp)NC(Me)CHC(Me)N(Dipp)...

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Panda A, Stender M, Wright RJ, et al. Synthesis and characterization of three-coordinate and related beta-diketiminate derivatives of manganese, iron, and cobalt. Inorg Chem. 2002;41(15):3909-16doi: 10.1021/ic025552s.
Panda, A., Stender, M., Wright, R. J., Olmstead, M. M., Klavins, P., & Power, P. P. (2002). Synthesis and characterization of three-coordinate and related beta-diketiminate derivatives of manganese, iron, and cobalt. Inorganic chemistry, 41(15), 3909-16. https://doi.org/10.1021/ic025552s
Panda, Arunashree, et al. "Synthesis and characterization of three-coordinate and related beta-diketiminate derivatives of manganese, iron, and cobalt." Inorganic chemistry vol. 41,15 (2002): 3909-16. doi: https://doi.org/10.1021/ic025552s
Panda A, Stender M, Wright RJ, Olmstead MM, Klavins P, Power PP. Synthesis and characterization of three-coordinate and related beta-diketiminate derivatives of manganese, iron, and cobalt. Inorg Chem. 2002 Jul 29;41(15):3909-16. doi: 10.1021/ic025552s. PMID: 12132915.
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Sc3N@C68: folded pentalene coordination in an endohedral fullerene that does not obey the isolated pentagon rule.

Angewandte Chemie (International ed. in English)

Olmstead MM, Lee HM, Duchamp JC, Stevenson S, Marciu D, Dorn HC, Balch AL.
PMID: 12596171
Angew Chem Int Ed Engl. 2003 Feb 24;42(8):900-3. doi: 10.1002/anie.200390237.

No abstract available.

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Olmstead MM, Lee HM, Duchamp JC, et al. Sc3N@C68: folded pentalene coordination in an endohedral fullerene that does not obey the isolated pentagon rule. Angew Chem Int Ed Engl. 2003;42(8):900-3doi: 10.1002/anie.200390237.
Olmstead, M. M., Lee, H. M., Duchamp, J. C., Stevenson, S., Marciu, D., Dorn, H. C., & Balch, A. L. (2003). Sc3N@C68: folded pentalene coordination in an endohedral fullerene that does not obey the isolated pentagon rule. Angewandte Chemie (International ed. in English), 42(8), 900-3. https://doi.org/10.1002/anie.200390237
Olmstead, Marilyn M, et al. "Sc3N@C68: folded pentalene coordination in an endohedral fullerene that does not obey the isolated pentagon rule." Angewandte Chemie (International ed. in English) vol. 42,8 (2003): 900-3. doi: https://doi.org/10.1002/anie.200390237
Olmstead MM, Lee HM, Duchamp JC, Stevenson S, Marciu D, Dorn HC, Balch AL. Sc3N@C68: folded pentalene coordination in an endohedral fullerene that does not obey the isolated pentagon rule. Angew Chem Int Ed Engl. 2003 Feb 24;42(8):900-3. doi: 10.1002/anie.200390237. PMID: 12596171.
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Synthesis and characterization of 2,6-Dipp(2)-H(3)C(6)SnSnC(6)H(3)-2,6-Dipp(2) (Dipp = C(6)H(3)-2,6-Pr(i)(2)): a tin analogue of an alkyne.

Journal of the American Chemical Society

Phillips AD, Wright RJ, Olmstead MM, Power PP.
PMID: 12022812
J Am Chem Soc. 2002 May 29;124(21):5930-1. doi: 10.1021/ja0257164.

The reaction of Sn(Cl)C(6)H(3)-2,6-Dipp(2) (Dipp = C(6)H(3)-2,6-Pr(i)()(2)) with a stoichiometric amount of potassium in benzene affords 2,6-Pr(i)()(2)-H(3)C(6)SnSnC(6)H(3)-2,6-Pr(i)()(2) (1) as dark blue-green crystals. The compound 1 is a tin analogue of an alkyne. It was characterized by (1)H and (13)C...

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Phillips AD, Wright RJ, Olmstead MM, et al. Synthesis and characterization of 2,6-Dipp(2)-H(3)C(6)SnSnC(6)H(3)-2,6-Dipp(2) (Dipp = C(6)H(3)-2,6-Pr(i)(2)): a tin analogue of an alkyne. J Am Chem Soc. 2002;124(21):5930-1doi: 10.1021/ja0257164.
Phillips, A. D., Wright, R. J., Olmstead, M. M., & Power, P. P. (2002). Synthesis and characterization of 2,6-Dipp(2)-H(3)C(6)SnSnC(6)H(3)-2,6-Dipp(2) (Dipp = C(6)H(3)-2,6-Pr(i)(2)): a tin analogue of an alkyne. Journal of the American Chemical Society, 124(21), 5930-1. https://doi.org/10.1021/ja0257164
Phillips, Andrew D, et al. "Synthesis and characterization of 2,6-Dipp(2)-H(3)C(6)SnSnC(6)H(3)-2,6-Dipp(2) (Dipp = C(6)H(3)-2,6-Pr(i)(2)): a tin analogue of an alkyne." Journal of the American Chemical Society vol. 124,21 (2002): 5930-1. doi: https://doi.org/10.1021/ja0257164
Phillips AD, Wright RJ, Olmstead MM, Power PP. Synthesis and characterization of 2,6-Dipp(2)-H(3)C(6)SnSnC(6)H(3)-2,6-Dipp(2) (Dipp = C(6)H(3)-2,6-Pr(i)(2)): a tin analogue of an alkyne. J Am Chem Soc. 2002 May 29;124(21):5930-1. doi: 10.1021/ja0257164. PMID: 12022812.
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Comparative Analysis of the Conformations of Symmetrically and Asymmetrically Deca- and Undecasubstituted Porphyrins Bearing Meso-Alkyl or -Aryl Groups.

Inorganic chemistry

Senge MO, Medforth CJ, Forsyth TP, Lee DA, Olmstead MM, Jentzen W, Pandey RK, Shelnutt JA, Smith KM.
PMID: 11669682
Inorg Chem. 1997 Mar 12;36(6):1149-1163. doi: 10.1021/ic961156w.

Conformational analysis of highly substituted porphyrins has potential implications for modeling the behavior of macrocycles in tetrapyrrole-containing protein complexes and during catalytic reactions. In order to study the influence of different substituent patterns on the conformation of the porphyrin...

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Senge MO, Medforth CJ, Forsyth TP, et al. Comparative Analysis of the Conformations of Symmetrically and Asymmetrically Deca- and Undecasubstituted Porphyrins Bearing Meso-Alkyl or -Aryl Groups. Inorg Chem. 1997;36(6):1149-1163doi: 10.1021/ic961156w.
Senge, M. O., Medforth, C. J., Forsyth, T. P., Lee, D. A., Olmstead, M. M., Jentzen, W., Pandey, R. K., Shelnutt, J. A., & Smith, K. M. (1997). Comparative Analysis of the Conformations of Symmetrically and Asymmetrically Deca- and Undecasubstituted Porphyrins Bearing Meso-Alkyl or -Aryl Groups. Inorganic chemistry, 36(6), 1149-1163. https://doi.org/10.1021/ic961156w
Senge, Mathias O., et al. "Comparative Analysis of the Conformations of Symmetrically and Asymmetrically Deca- and Undecasubstituted Porphyrins Bearing Meso-Alkyl or -Aryl Groups." Inorganic chemistry vol. 36,6 (1997): 1149-1163. doi: https://doi.org/10.1021/ic961156w
Senge MO, Medforth CJ, Forsyth TP, Lee DA, Olmstead MM, Jentzen W, Pandey RK, Shelnutt JA, Smith KM. Comparative Analysis of the Conformations of Symmetrically and Asymmetrically Deca- and Undecasubstituted Porphyrins Bearing Meso-Alkyl or -Aryl Groups. Inorg Chem. 1997 Mar 12;36(6):1149-1163. doi: 10.1021/ic961156w. PMID: 11669682.
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cis and trans Forms of a binuclear subphthalocyanine.

Angewandte Chemie (International ed. in English)

Fukuda T, Stork JR, Potucek RJ, Olmstead MM, Noll BC, Kobayashi N, Durfee WS.
PMID: 12203535
Angew Chem Int Ed Engl. 2002 Jul 15;41(14):2565-8. doi: 10.1002/1521-3773(20020715)41:14<2565::AID-ANIE2565>3.0.CO;2-G.

No abstract available.

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Fukuda T, Stork JR, Potucek RJ, et al. cis and trans Forms of a binuclear subphthalocyanine. Angew Chem Int Ed Engl. 2002;41(14):2565-8doi: 10.1002/1521-3773(20020715)41:14<2565::AID-ANIE2565>3.0.CO;2-G.
Fukuda, T., Stork, J. R., Potucek, R. J., Olmstead, M. M., Noll, B. C., Kobayashi, N., & Durfee, W. S. (2002). cis and trans Forms of a binuclear subphthalocyanine. Angewandte Chemie (International ed. in English), 41(14), 2565-8. https://doi.org/10.1002/1521-3773(20020715)41:14<2565::AID-ANIE2565>3.0.CO;2-G
Fukuda, Takamitsu, et al. "cis and trans Forms of a binuclear subphthalocyanine." Angewandte Chemie (International ed. in English) vol. 41,14 (2002): 2565-8. doi: https://doi.org/10.1002/1521-3773(20020715)41:14<2565::AID-ANIE2565>3.0.CO;2-G
Fukuda T, Stork JR, Potucek RJ, Olmstead MM, Noll BC, Kobayashi N, Durfee WS. cis and trans Forms of a binuclear subphthalocyanine. Angew Chem Int Ed Engl. 2002 Jul 15;41(14):2565-8. doi: 10.1002/1521-3773(20020715)41:14<2565::AID-ANIE2565>3.0.CO;2-G. PMID: 12203535.
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