氫氣在燃燒後只會產生水而不產生溫室氣體之二氧化碳，可謂一種潔淨能源。 生質能源是屬於碳中性(Carbon neutral)型之利用方式，因此本研究著眼於如何建構一個操作簡便的共代謝系統，將生質料源從微生物之發酵反應中釋放氫氣出來。 實驗的主要方法是利用好氧性的Bacillus thermoamylovorans 與厭氧性的Clostridium butyricum 共培養分解廢紙漿以生產氫氣。廢紙漿是混合的基質，內富含纖維素、並含一些油墨及少許雜質。利用Bacillus thermoamylovorans 是好氧菌，同時也能將廢紙漿中的纖維素轉換成還原醣的特性，將原本有氧的環境轉換成絕對厭氧的環境，並將廢紙漿中的纖維素轉化成Clostridium butyricum 可以利用的還原醣。如此一來，原本不利於Clostridium butyricum 生長的環境，卻能透過簡單的共培養方式創造出有利於Clostridium butyricum 生長的環境並產生氫氣。除此之外，我們也對不同碳源、不同的植菌量、不同的氧氣量，比較其產氫能力差異，發現增加氧氣量可以提升最後的產氫量大約2.7 倍。 ;Our major goal is to develop a cost-effective biohydrogen production system by the co-culturing of Bacillus thermoamylovorans and Clostridium butyricum. The aerobic Bacillus thermoamylovorans will consume oxygen and converse waste paper pulp into reductant-sugar and the anaerobic Clostridium butyricum will generate hydrogen after oxygen is consumed. With the increase of aeration, the aerobic Bacillus thermoamylovorans growsappropriately leading to more biohydrogen production. However, in enhanced aeration condition, the Bacillus thermoamylovorans will consume sugars that can offer for the Clostridium butyricum. So we can conclude that the control of oxygen is the key point for the system to operate.

We can prove 鬼腳圖 have an one-to-one characteristic; it is mean that you can not design a 鬼腳圖 which will make two starting point to the same end. We also can prove you can design any 鬼腳圖 you want; you can predict a result, and you can design a 鬼腳圖 which suit the result, no matter what the result it is. We can design any 鬼腳圖 we want, but it possibly becomes very big and complicated. We develop a method to make it become briefer. According to the method, we make a function that can design the 鬼腳圖 you want in a very short time. You predict a result in computer, and the\r function will design a 鬼腳圖 which suit the result, and it will be the briefest. 吾人已經可以證明鬼腳圖具備一對一的性質，意思就是：不可能從兩個起點開始畫線，最後到同一個終點上。吾人亦證明：鬼腳圖的結果沒有限定：同一組初始條件可以轉換成任何一組結果。而同一組結果也有許多種不同的畫法，顯示鬼腳圖的畫法不具唯一性。即使如此，畫出來的鬼腳圖可能過於複雜，於是吾人又發展出簡化鬼腳圖的方法，可畫出較簡潔的鬼腳圖。吾人並根據這種化簡方式編出一套程式，只要將欲得的結果輸入，電腦就可以畫出最簡潔的鬼腳圖。

Lantana is a very common plant in our lives. It grows easily and it has a long florescence and various colors. The colors of particular types of lantana alter as the changing florescence. In this experiment, paper chromatography, high-performance liquid chromatography, SDS-gel electrophoresis, the measurement of petal cellular pH values, and the comparative study of forms of trachoma on the epidermal cells of petals are exerted in order to explore factors that change the colors of the lantanaThe findings are as follows:\r (1)Lantana’s colors have inseparable relationships with the compositions of anthocyanins and flavonoids, but not with the pH values of petal cells.(2)The anthocyanins of petal cells are cyanidm, with glycosides as well.(3)Beside the differences in the compositions of pigments, the forms of trachoma on the epidermis of the petal, cone-like or caniniform, can also be used to distinguish different types of lantana, because the trachoma can influence the reflections of light from the epidermis of the petals and also affect colors of the flowers.(4)The result of SDS-gel electrophoresis shows that the biochemical pathways of petal cells in all species of lantana are similar, so we assume that there is mutant in the series of synthesizing enzyme when the anthocyanins of petal cells are formed, and thus, there are no anthocyanins appearing in the yellow and white species of lantanaThe results above are helpful for the understanding and discovering of lantana’s biological mechanisms, and can be used to create new types of lantana and to make further study of the metabolism of lantana’s complete anthocyanin’s biochemical pathway馬纓丹(Lantana ssp.)是常見景觀植物，容易栽種、花期長、花色多，且有些品系花色會隨著花期而變化。本實驗利用濾紙色層分析、高效能液相層析、SDS-gel電泳、細胞pH值測定及花瓣表皮細胞之毛茸(trichoma)型態之比較等方法探討馬纓丹花色之不同及變化的原因。結果顯示: (1)馬纓丹的花色及花色變化與花青素(anthocyanins)和類黃素(flavonoids)之組成有密切關係，而與花瓣細胞內pH值無關。(2)花瓣中所含花青素為矢車菊色素(cyanidm)，並且具有配醣基(glycoside)。(3)花瓣表皮細胞之毛茸型態，如圓錐形或犬牙型，會影響光的反射，進而影響花色，所以毛茸型態可做為區分馬櫻丹品系之特徵。(4)SDS-gel電泳的結果顯示，馬櫻丹各品系的花瓣細胞生合成類似，推測花瓣細胞產生花青素的一系列酵素中，已有突變發生，而造成黃色、白色品系無花青素。以上結果有助於了解馬纓丹花色變化之機制，可將其應用於改良出新的馬櫻丹之品系，或更深入研究馬櫻丹花青素完整生成代謝路徑。

We consider a game played with chips on a strip of squares. The squares are labeled, left to right, with 1, 2, 3, . . ., and there are k chips initially placed on distinct squares. Two players take turns to move one of these chips to the next empty square to its left. In this project, we study four different games according to the following \r rules: Game A: the player who places a chip on square 1 wins;Game B: the player who places a chip on square 1 loses;Game C: the player who finishes up with chips on 12 . . . k wins;Game D: the player who finishes up with chips on 12 . . . k loses. After studying the cases k = 3, 4,5 and 6 for Game A and the relation among these four games, we are led to discover the winning strategy of each game for any positive integer k. The strategies of Games A, B and C are closely related through a forward or backward shifting in position. We also found that such strategies are similar to the type of Nim game that awards the player taking the last chip. Game D is totally different from the rest. To solve this game, we investigate the Nim game that declares the player taking the last chips loser. Amazingly, the strategies of two Nim games can be concisely linked by two equations. Through these two Nim games, we not only find the winning strategy of Game D but also the precise relation between Game D and all others.\r 去年我研究一個遊戲：有一列n個的方格中，從左至右依序編號為1,2,3,....n。在X1個、第X2個、第X3個格子中各放置一個棋子。甲乙二個人按照下列規則輪流移動棋子：\r 一、甲乙兩個人每次只能動一個棋子(三個棋子中任選一個)。遊戲開始由甲先移動動棋子。二、甲乙兩個人每次移動某一個棋子時，只能將這個棋子移至左邊最近的空格(若前面連續有P個棋時可以跳過前面的P個棋子而且只能跳一次)，而且每個方格中最多只能放一個棋子。\r 研究這個遊戲問題時，我討論四種不同"輸贏結果"的規定：甲乙兩個人中，A誰先將三個棋子中任意一個棋子移到第一個方格，誰就是贏家。B誰先將三個棋子中任意一個棋子移到第一個方格，誰就是輸家。C誰先不能再移動任何棋子，誰就是輸家。D誰先不能再移動任何棋子，誰就是贏家。\r 當"輸贏結果"的規定採用ABCD時─我們稱為遊戲ABCD。今年我將把這個遊戲問題中棋子的個數由三個推廣到一般K個情形之後，再繼續研究遊戲的致勝策略，同時也將研究遊戲ABCD之間的關係。

政府全面換發國民身分證，並訂定新式身分證之規格，以防範遭不法偽造之情事，確保民眾權益。然而其中的照片規格，有十多條規格的限定，若用傳統的辨別方式，近1876 萬張照片是否合乎規定，那將耗費多少的人力呢？於是本次研究主題「新式國民身分證相片規格驗證暨浮水印防偽系統」即產生，設計一套程式，提高換發國民身分證的工作效率及確保換證使用相片的正確度。並且延伸研究出使用內崁式的數位浮水印〈Digital Watermarks〉，將全國民眾的身分證照片統一建立資料庫，並自動加入個人資料浮水印。日後，照片只需透過本程式分析，即可知道其姓名、身分證字號、有無犯罪前科等個人資料。希望藉此達到降低偽造身分證之犯罪率，以保護民眾之權利。 The government is launching to renew national identification cards with new norms, to avoid fake ones. However, there are more than ten limits on photos, it could be wasting time to discern by people. Thus, I launched a research on "The xamination on new national ID card photos and watermark forgery-proof system". The program will help both to enhance efficient renewal process and to use correct photos. Also we developed the embeded Digital Watermark technology, which would create a database for ID cards of the nation and could add personal infomation automatically. With the help of the program, simply run the photo analysis, we could find out the names, ID number, criminal background, etc.We hope to decrease crimes via fake ID cards, and protect the national right.

目前生物學知識認為雉科鳥類的性別，在卵受精後即決定(WZ型)，不受環境的影響，但是在本組一連串的實驗中發現，雉科鳥類的性別與孵化的溫度變化有非常大的影響，一般宮廷雞的孵化條件在濕度55％RH及溫度98℉～99℉，在此孵化條件下宮廷雞的子代♀：♂=1：1，若溫度降為97℉的孵化條件下所得子代♀性佔93％，倘若溫度升高為100℉的孵化條件下所得子代♂性佔92％，可見在比正常孵化溫度高的環境下宮廷雞的受精卵會轉變為♂性，而比正常孵化溫度低的環境下孵化的宮廷雞受精卵卻會轉變為♀性，本實驗續做了六代，結果大致相似，由此可以證明控制孵化溫度可以改變宮廷雞的性別，這一行為，可能與Z染色體上一個溫度依賴型的連鎖基因(DMRT1)之表現有關。 ;The temperature of hatching can affect Chinese silkys's sex It is now established that the sex of Pheasants is determined when the egg is impregnated, rather than by environmental factors. However, in a series of experiments, we find that the sex of Pheasants is strongly related to the temperature of hatching. In the normal hatching condition (humidity:55% RH ,temperature: 98.5℉), the ratio of female and male offspring of Chinese silkys is 1:1. If the temperature is lowered to 97℉, the female offspring occupies a proportion of 93%. If the temperature is raised to 100℉, the male proportion will reach 92%. We can thus derive the conclusion: the impregnated eggs of Chinese silkys will be transformed to male at a temperature higher than the normal one, while a lower temperature than the normal one will cause the impregnated eggs to be female. The experiments have been conducted through six generations of Chinese silkys, and the results are practically the same. This indicates that temperature changes can affect gender, This may be related to a Z-linked of DMRT1 gene on the DNA, which is temperature-dependent.

Poly(ADP-ribose) polymerase-1 (PARP-1)是一個細胞核內的酵素，它可以被因DNA damage\r 而形成的DNA片段活化，並將NAD(+)上的ADP-ribose轉載到結合蛋白質。這些結合蛋白質對\r 於DNA的合成、DNA的修補、以及細胞週期的調控都有關係。因此，PARP-1被認為是維持基\r 因完整性的重要角色。根據初步的研究，抑制PARP-1的活性對許多疾病的治療都可能有效，\r 其中包括癌症、心臟病、中風、糖尿病、發炎以及反轉錄病毒的感染。然而，以藥物抑制一\r 個對DNA修補這麼重要的酵素會有什麼潛在的問題呢？為了要得到解答，我們需要進一步了\r 解PARP-1在DNA damage反應的機能。在這一份報告中，我製造了一個失去活性的PARP-1突變\r 種，即E988K。經過對E988K詳細的研究，我將比較及分析PARP-1野生型與E988K之間不一樣\r 的互動蛋白質，希望能對PARP-1所控制的DNA修補有更進一步的了解。\r \r \r Poly(ADP-ribose) polymerase-1 (PARP-1) is a nuclear enzyme activated by DNA strand breaks\r during DNA damage response and catalyzes the transfer of ADP-ribose units from the substrate NAD(+)\r to acceptor proteins. These acceptor proteins involve in modulation of chromatin structure, DNA\r synthesis, DNA repair, transcription, and cell cycle control. Thus, PARP-1 is believed to play an\r important role in maintaining genome integrity through modulation of protein-protein and protein-DNA\r interactions. PARP-1 has been the target for design of inhibitors for over twenty-five years. Inhibitors of\r the activity of PARP-1 have been claimed to have applications in the treatment of many disease states,\r including cancer, cardiac infarct, stroke, diabetes, inflammation and retroviral infection. However, are\r there potential problems associated with inhibition of this DNA-repair enzyme? To answer this question,\r we need to further understand the biological function of PARP-1 during DNA damage response. In this\r report, an enzyme dead mutant (E988K) of PARP-1 was generated. Detailed studies of E988K show that\r E988K could be used in the following studies. Compare and identify the different associated proteins of\r PARP-1 wild-type and E988K will shed light into the molecular mechanism of PARP-1-mediated DNA\r repair.

NO.58-01 2019 FEB | 科學研習期刊目錄 本期專題 運用科技的物理教學 智慧型科技與行動學習： 以手機APP為例 | 賈至達 綠能數位與實作教材 之發展與運用 | 盧玉玲 蠟燭燃燒實驗的IoT 之旅 | 李柏翰 、江政龍、蘇萬生 智慧型手機立體影像STEAM實作教材 | 洪連輝、張益嘉 運用Arduino探究視覺暫留 | 陸健榮、鄭依佩 科學探究隨手做：手機感應器的物理原理與教學上的應用 | 盧政良 教學現場 動手玩科技：射箭Robot自己做 | 施皇羽、許弘叡 量子力學之美：電腦叢集計算在附中 | 李柏翰 科學新知 淺談「智慧電網」 | 蔡振明 特約專欄 變色龍 | 游森棚 帶得走的STEAM課程設計：古機械鐘創意課程 | 黃琴扉 趣讀科普，昇華閱讀，活化STEM腦 | 劉淑雯 科普活動報導 看得獎影片 學有趣科學 | 李名揚 科教館GO好玩 電漿球演示融入科學劇的情節歷程--以｢電漿球｣演示為例 | 陳香微 總召集人的話 本刊自本期起改為雙月刊，於「臺灣網路科教館」網址刊登，文章方向將更緊扣STEAM教育與國中小物理、化學、生物、地科、科技、數學六大領域或分科。除將於「本期專題」和「教學現場」單元刊登和12年國教課程與教學相關文章外，亦結合科教館「科普傳播中心」做更多元化的分享與傳播。物理科召集人是國立彰化師範大學物理學系吳仲卿教授，「本期專題」推出「運用科技的物理教學」專題。 「本期專題」共有六篇文章：〈智慧型科技與行動學習：以手機APP為例〉一文以智慧型手機的APP為主軸，論述智慧型科技在「行動學習」的應用，以及在科學學習的幾個面向。〈綠能數位與實作教材之發展與運用〉一文分享作者研究室所研發的「綠色能源」數位教材，教材係整合情境式數位學習與實作探究而成，以風力發電為主題。〈蠟燭燃燒實驗的IoT之旅〉一文帶領讀者利用國中理化課程單元--密閉容器蠟燭燃燒實驗，結合國家晶片系統設計中心開發的MorSensor測定晶片，設計一套創新的實驗流程。〈智慧型手機立體影像STEAM實作教材〉一文作者分享其整合STEAM教育精神，所開發出主題為「立體視覺與虛擬實境」的一套光學領域課程與教材。〈運用Arduino探究視覺暫留〉一文分享如何運用新科技--開源微控制器，針對視覺暫留現象進行定量的探究與實作，同時訓練學生測量與分析以及程式與電路等跨領域的基本素養。〈科學探究隨手做：手機感應器的物理原理與教學上的應用〉一文分享利用手機進行數位量測教學的的經驗與建議。 「教學現場」刊登兩篇文章：〈動手玩科技：射箭Robot自己做〉一文分享在國小利用木工課程搭配microbit的程式設計，進行「射箭Robot」的設計經驗。〈量子力學之美：電腦叢集計算在附中〉一文分享在高中開授多元選修課程「量子力學之美，電腦叢集計算」的經驗與成果。 「科學新知」刊登〈淺談「智慧電網」〉一文，介紹智慧電網的三大要件：智慧電表，資訊、通信與自動化系統，和儲能系統。 「特約專欄」刊登三篇文章：〈變色龍〉拋出兩隻不同顏色的變色龍相遇會同時變成第三種顏色的問題。〈帶得走的STEAM課程設計：古機械鐘創意課程〉一文分享跨校、跨領域、跨單位整合，創建一系列古機械教具與教材教法的經驗。〈趣讀科普，昇華閱讀，活化STEM腦〉一文從STEM教育觀點介紹四種類型的科普書籍。 「科普活動報導」刊登〈看得獎影片 學有趣科學〉一文，報導已有公播版的「永不妥協－實驗室的挑戰故事」系列影片。 「科教館GO好玩」刊登《電漿球演示融入科學劇情節歷程探討—以｢電漿球｣的演示為例》一文，分享科教館科學劇「今天我們去哪兒」，將展品｢電漿球｣的演示融入劇情中，彰顯科學與藝術跨領域整合的效果與心得。 總召編輯委員 - 李隆盛 關於本刊 出版單位：國立臺灣科學教育館 發行人：陳雪玉 總召集人：李隆盛 編輯委員： 物理科吳仲卿/陳耀榮/李柏翰/盧玉玲 | 化學科古建國/許良榮/王伯昌/林如章/周金城 | 生物科王美芬/蕭世輝/陳建志/郭淑妙 | 地球科學許民陽/王郁軒/李文禮 科技科張玉山/汪殿杰/林育沖/趙珩宇 | 數學科李源順/鄧家駿/溫世展/張宮明 | 跨領域學科李名揚/連信仲 | 特約專欄 游森棚/黃琴扉/劉淑雯 策劃：曾聰邦 主編：錢康偉 本月專題特約主編：吳仲卿 編輯：吳郡怡 網頁設計編輯：施曉恬/陳璽君 投稿規範請來信詢問：article@mail.ntsec.gov.tw

儘管鍺在電子工業上被廣泛運用，但對於暴露在鍺化合物所產生的毒害則尚未被詳細的探討。在探討鍺對細胞所產生的生理影響中，我們使用了二氧化鍺 ( GeO2）和有機鍺（ Ge-132 ）。由實驗結果顯示， GeO2，會造成人類子宮上皮癌細胞（ A 431 ) 及巨噬細胞株（ Raw264.7 ）死亡，而 Ge -132 對細胞生長則不造成任何影響，為了進一步了解鍺引起細胞死亡是否是經過細胞凋亡（apoptosis ) ，我們將鍺處理過的細胞進行染色體 D NA 的分析，結果發現細胞中 DNA 染色體沒有斷裂。由先前 Huang 等人於 1999 年的研究結果顯示，砷對細胞所造成的毒性是經由有絲分裂活化酵素（ MAPK ）傳導路徑，所以為了解鍺誘導細胞死亡的路徑，我們亦分析 MAPK 傳導路徑是否亦參與其中，我們發現 GeO2加入 A431 細胞後，會活化有絲分裂活化酵素中的 ERK ，但對JNK 及 p38 皆無影響，在對蛋白質表現方面，轉錄因子 c-Jun 的蛋白質表現也是隨著GeO2加入的時間增加而上升。 GeO2加入 Raw 264 . 7cell 後，會造成 JNK 、 ERK 的活化，同樣的轉錄因子 c- Jun 也會增加，由此一結果得知鍺對細胞的影響會因細胞的不同而有所差異，為了分析自由基是否參與砷及鍺所造成細胞死亡的過程，我們分析在 A431 細胞中可產生的 NO 的可誘導性 nitric oxide synthase ( iNOS ）的表現，我們發現氧化鍺及砷都會誘導 iNOS 的表現量增加。綜合以上結果，可能顯示氧化錯可能會經由 M A PK 訊息傳遞路徑來促使細胞的死亡，並且 iNOS 亦可能參與此過程。就我們所知，這是第一個提出重金屬所造成的毒害可能會經由 iNOS 來誘導產生的研究。 Despite the extensive use of germanium (Ge) in the electronic industry and optical devices, the potential risks of exposure to germanium compounds have not been evaluated. The effects of germanium on cell physiological functions were studied. We first asked if germanium oxide (GeO2) or carboxyethylgermanium (Ge-l32) could affect cell viability. We found that GeO2, but not Ge-l32, reduced cell viability in a dose-dependent manner in epidermoid carcinoma A43 I and macrophage Raw 264.7 cells. In order to test whether apoptosis contributes to germanium cytotoxicity, DNA fragmentation was evaluated in A43 1 and Raw 264.7 cells treated with GeO2 or Ge-132, respectively. We found that neither GeO2 nor Ge- 132 had effect on chromosomal DNA fragmentation. Previous studies by Huang (1999) et al indicated that sodium arsenite (NaAsO2) cytotoxicity is mediated through mitogen-activated protein kinase (MAPK) pathways. In order to study the mechanism(s) by which GeO2 mediates cell death, we analyzed the signal transduction pathways triggered by GeO2 We found that GeO2 stimulated the extracellular signal-regulated kinase (ERK) activity and transcription factor c-Jun in a time-dependent manner, but not c-Jun amino-terminal kinasc (JNK), or p38 MAPK in A431 cells. Treatment of the Raw 264.7 cells with GeO2, induced activities of ERK, JNK and c-Jun in a time-dependent manner. Collectively, these results suggested that GeO2 effects might be cell type specific. To test whether free radicals were involved in NaAsO2 or GeO2 mediated cell death, the expression of inducible nitric oxide synthase (iNOS), which produced the NO free radical, was determined in A431 cells treated with NaAsO2 or GeO2. We found that expression of iNOS was induced in a time-dependent manner in NaAsO2 or GeO2-treted A431 cells. Taken together, our results indicated that GeO2-induccd cell death may be mediated through MAPK signal pathways and that iNOS may contribute to NaAsO2 or GeO2 mediated cell death. To our knowledge, this is the first report that iNOS may contribute to heavy metal mediated cytotoxicity.

高二上學期化學第一章，就討論到電子組態及原子光譜，雖然課本上有美麗的光譜插圖，但是觀念還是覺得十分抽象。所以老師為了提高我們學習的興趣，在實驗課中教我們自製簡易分光器，實際去觀賞各種光源及有色溶液的光譜，觀賞過程我們發現下列的問題：（1）為何一般離子是帶狀光譜，而MnO4- 光譜卻像線光譜？（2）MnO4- （深紫）和Mn2+（幾近無色），兩者顏色差異很大。是否與Mn 離子是否單獨存在有關係？（3）而另外CrO42- （黃）、Cr2O72- （橙）和Cr3+（深藍色），三者顏色差異，是否與MnO4- 和Mn2+原因類似？為了尋找這些答案，於是開始了這個題目研究的過程。這期間我們花了很多時間與方法，嘗試將肉眼觀察到的影像，在自設的簡單暗房中，將光柵卡在數位相機的鏡頭前，以腳架或翻拍架拍攝下來。另外我們也應用到高三上學期平衡常數測定實驗中比色法的觀念，以及物理學上單狹縫繞射的觀念，使課本中的理論與實驗研究相互結合！最後我們藉分光光譜儀測定各有色溶液的可見光吸收光譜，再去定量分析這些有色溶液的顏色深淺，並查閱相關的文獻資料。最後發現MnO4-應該是一種電荷傳遞的遷移，所引起特別深顏色的現象。 至於CrO42- 、Cr2O72- 和Cr3+三者顏色比較上是否和MnO4- 和Mn2+一樣的情形？我們推測應該也是如此！初見Cr3+有很深的顏色時，的確嚇了一跳，不過最後我們還是從它們的可見光吸收光譜中發現： CrO42- 、Cr2O72- 在λmax 的吸光度比Cr3+還要大！但是為何肉眼觀察到的Cr3+顏色會比較深？那是因為我們視覺上對藍綠色比較敏感的緣故！請參考表一。 We have discussed some electronic configurations and atomic spectrums in chemistry class. Although there were a few beautiful spectrums in textbook , but it’s difficult to understand. So we made a simple spectroscope by ourselves to observe spectrums of different light source and color solution . After some observation we have found some problems below ： （1）Why the spectrum of color solution is band spectrum , but the spectrum of permanganate ion (MnO4- ) like line spectrum？ （2）MnO4- （deep purple）and Mn2＋（pink）, their color are different very much. Is it because of the lone existence and binding with oxygen atom of manganese ion? （3）Additionally CrO42- （yellow）、Cr2O72- （orange）、Cr3+（deep blue），Are their color’s difference same as MnO4- and Mn2+？ In order to solve it , we started to do the reasrech. We tested different methods much time to record . Finally , We found a good method . That’s placed a grating in front of the digital camera len to take single slit diffraction spectrum pictures in the dark space. Additionally we used spectrophotometer to measure the visible light absorption spectrum. We compared and matched with single slit diffraction spectrums and visible light absorption spectrums. Then we found the intense color of MnO4- due to charge transfer in reference book. How about color’s difference between CrO42- 、Cr2O72- 、Cr3+group and MnO4、 Mn2+ group? We guess they had the same result . We can find the λmax of CrO42- 、Cr2O72- is larger than Cr3+ from the absorption spectrum. But the observation from naked eyes was inverse . This is owing to our vision is more sensitive to blue color. Refer Table 1.

The research mainly discuss the influence on the rate of zinc iodine with different solution as catalytic agent. We use water, acid water, ethanol methanol acid ethanol, and acid methanol and so on as different solution to participate in the process of an equation： Zn+I2 → ZnI2 to work out the variation of the product's amount. Besides, we also change the proportion of Zinc and Iodine to discuss the difference between the proportion of reactant and the product's amount. The result shows that the product of this equation is ZnI2 not Zn(I3)2. Ethanol and methanol have the same effect as water to accelerate the process of the equation. We find out that this reaction get higher product's amount in acid condition. Also, put the mass Zinc with the mass iodine can get higher product's amount, Furthermore, acid in specific range (0.01M—1.00M), the denser the acid is, the higher product's amount we get. But how the water as catalytic agent work in the reaction is the direction we can research deeply in the days to come. 鋅和碘作用生成碘化鋅的反應，是用水作為催化劑，然而一小滴水卻使這個反應劇烈進 行，我們嘗試了多種和水具有相同作用的催化劑，由於反應時間極短不易測量，我們考慮由 產率部分著手，讓原本只需一小滴的水〈催化劑〉改為此反應的溶劑，計算其產率的變化。 實驗分為三部分，第一部份先是改變不同的溶劑，讓鋅和碘在不同溶劑〈水、酸化水、乙醇、酸化乙醇、甲醇、酸化甲醇〉下反應，計算出產率的變化，我們發現在酸中的產率的確較不加酸者來得高。第二部分我們改變加入鋅和碘的量，改變鋅和碘的比例，讓鋅由過量到成為此反應的限量試劑，觀察其產率的變化，我們發現碘作為限量試劑較鋅作為限量試劑的產率高。由於此反應在酸中產率較高，但酸的濃度高低是否又會影響產率呢？我們繼續第三部分的實驗，改變酸的濃度，讓此反應在不同的酸化水濃度的溶劑下反應，討論產率和酸濃度的關係，我們發現在一定範圍內〈0.01M~0.5M〉，酸的濃度越高，產率亦越高。 實驗方法是將鋅和碘置入同一試管中反應，並使其在不同溶劑中反應，接著離心，將碘化鋅水溶液與未反應完的反應物分離，將所得的碘化鋅水溶液使用結晶法得到碘化鋅晶體，秤重並計算其產率。

在本實驗中，我們合成了三個新的鋅的幾何異構物：trans-facial-[Zn(dipica)₂]Cl2.CH3OH(dipica=dipicolylamine，C12H13N3，雙(2吡啶甲基)胺)trans-facial-[Zn(dien)2]Cl2(dien=diethylenetriamine，C4H14N3，二乙基三胺)及反式-[Zn(demn)2Cl2](demn=N,N’-dimethylethylenediamineC4H12N2，N,N'-二甲基乙二胺)。本實驗的特色皆在室溫下反應，採用擴散法培養晶體。trans-facial-[Zn(dipica)22]Cl2.CH3OH晶體為三斜晶系，晶格常數a=8.8269(6)Å, b=8.9908(6)Å, c=10.0292(6)Å,α=76.715(1)。,β=81.232(1)。,γ=67.753(1)。;其空間群為P1，可信度R=0.025,Rw=0.0697。六配位的陽離子，其結構為扭曲八面體，兩個含氮三牙基(dipica)trans-facial配位，赤道面(ZnN(1)N(2)N(1A)N(2A))由兩個含吡啶環之氮(N(1)、N(1A))及兩個飽和胺之氮(N(2)、N(2A))所組成。主軸為兩個吡啶環之氮所組成。兩個含氮三牙基(dipica)與鋅的咬合角皆為84.5。。trans-facial-[Zn(dien)2]Cl2晶體為單斜晶系，晶格常數為a=11.3050(3)Å,b=10.9264(3)Å, c=12.6147(3)Å,β=92.884(1)。;其空間群為P21/c，可信度R=0.0191，Rw=0.0484。六配位的離子，其結構為扭曲八面體，兩個含氮三牙基(dien)與鋅的咬合角為156°、157°。反式-[Zn(dmen)2Cl2]晶體為單斜晶系，晶格常數 a=10.3397(4)Å,b=8.5916(4)Å,c=7.9774(3)Å,β=100.520(1)°;其空間群為C2/m，可信度R=0.0266，Rw=0.0686。其結構為八面體，鋅原子四個氮原子組成赤道面(ZnN(1)N(1A)N(1B)N(1C))，兩個氯原子位於此平面的兩側。兩個含氮雙牙基(dmen)與鋅的咬合角皆為83.0(1)Å。 In this study, we have synthesized three new geometrical isomers of zinc(II)complexes: trans-facial-bis(dipicolylamine)zinc(II)chloride-mathanol(1/2)(trans-fac-[Zn(dipica)2]Cl2.2CH3OH), trans-facial-bis(ethylenetriamine)zinc(II)chloride(trans-fac[Zn(dien)2]Cl2)and trans-bis(N, N'-dimethylethylenetriamine)zinc(II)chloride(trans-[Zn(dmen)2]Cl2). The crystals suitable for X-ray diffraction were obtained by slow diffusion of ether to solution of the products. There molecular strctures determined by X-ray diffraction. The complex trans-fac-[Zn(dipica)2]Cl2.2CH3OH crystallizes in the triclinic space group P 1 with a=8.8269(6)Å, b=8.9908(6)Å, c=10.0292(6)Å,α=76.715(1)。,β=81.232(1)。,γ= 67.753(1)。, for Z=1. The R value is 0.0259 for 3286 significant reflections. In the hexacoordinate cation, the two tridentate dipicolylamine ligands are trans-facially coordinated with two pyridine nitrogens and two secondary amine nitrogens situated on four positions in a basal plane(ZnN(1)N(2)N(1A)N(2A)). The remaining two pyridine nitrogens constitute the axis in a distorted octahedra structure. Colorless trans-fac-[Zn(dien)2]Cl2 crystallizes the monoclinic space group P21/c with a=11.3050(3)Å, b=10.9264(3)Å, c =12.6147(3)Å,β=92.884(1)。,and Z=1. The R value is 0.0191 for 3285 significant reflections. The zinc(II) atom has distorted octahedra coordination, in which the ligands are bound in a trans-facial configuration. Colorless trans-[Zn(dmen)2Cl2] crystallizes the monoclinic space group C2/m with a=10.3397(4)Å, b= 8.5916(4)Å, c=7.9774(3)Å,β=100.520(1)。, and Z=2. The R value is 0.0266 for 856 significant reflections. The zinc(II)atom of trans-[Zn(dmen)2Cl2]is six coordinate with 4 nitrogens of bidentate dmen forming a basal plane(ZnN(1)N(1B)N(1A)N(1C)),and two chlorines on the axial sites completing an octahedra structure.